A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645737



Internal ID6685798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36533223..36534274hg38UCSC Ensembl
Innerchr20:36533223..36534274hg38UCSC Ensembl
Outerchr20:36532955..36534496hg38UCSC Ensembl
chr20:35161626..35162677hg19UCSC Ensembl
Innerchr20:35161626..35162677hg19UCSC Ensembl
Outerchr20:35161358..35162899hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381052
hg191052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16179803, essv16179809, essv16179808, essv16179804, essv16179802, essv16179810, essv16179807, essv16179801, essv16179805, essv16179806
SamplesHG03518, NA18498, HG02943, NA19462, NA19236, NA20299, HG03473, HG02938, NA18505, NA19312
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645737
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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