A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645712



Internal ID6685774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35167207..35174665hg38UCSC Ensembl
chr20:33755010..33762468hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg387459
hg197459
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16178640, essv16178645, essv16178642, essv16178641, essv16178644, essv16178639, essv16178637, essv16178643, essv16178646, essv16178638
SamplesHG00626, HG02061, HG02050, HG02512, NA18638, HG03391, NA18536, HG03469, NA18636, HG00628
Known GenesPROCR
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645712
Frequency
Sample Size2504
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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