A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645059



Internal ID6685122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3898170..3904490hg38UCSC Ensembl
Innerchr20:3898183..3904477hg38UCSC Ensembl
Outerchr20:3898157..3904503hg38UCSC Ensembl
chr20:3878817..3885137hg19UCSC Ensembl
Innerchr20:3878830..3885124hg19UCSC Ensembl
Outerchr20:3878804..3885150hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg386321
hg196321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16122284, essv16122286, essv16122288, essv16122285, essv16122275, essv16122274, essv16122270, essv16122258, essv16122283, essv16122290, essv16122292, essv16122291, essv16122261, essv16122273, essv16122272, essv16122277, essv16122280, essv16122262, essv16122266, essv16122254, essv16122265, essv16122267, essv16122260, essv16122257, essv16122281, essv16122279, essv16122256, essv16122287, essv16122276, essv16122264, essv16122282, essv16122255, essv16122269, essv16122268, essv16122263, essv16122289, essv16122259, essv16122271, essv16122278
SamplesHG04096, NA19794, NA20877, HG03731, HG03738, HG01188, HG01456, NA19684, HG00737, NA19669, HG01177, HG03765, NA19720, HG03986, HG03777, NA18645, NA20854, HG00268, HG02165, HG01029, NA18537, HG01447, HG03829, NA20903, HG04173, NA19740, HG02031, HG00864, HG03743, HG03598, HG02089, HG03809, HG03708, HG01131, HG02685, NA19783, NA20847, NA19726, HG00759
Known GenesPANK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645059
Frequency
Sample Size2504
Observed Gain0
Observed Loss39
Observed Complex0
Frequencyn/a


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