A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645730



Internal ID7032478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36075856..36077347hg38UCSC Ensembl
Innerchr20:36075857..36077347hg38UCSC Ensembl
Outerchr20:36075856..36077348hg38UCSC Ensembl
chr20:34663778..34665269hg19UCSC Ensembl
Innerchr20:34663779..34665269hg19UCSC Ensembl
Outerchr20:34663778..34665270hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381492
hg191492
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16179769, essv16179771, essv16179768, essv16179767, essv16179766, essv16179765, essv16179772, essv16179770
SamplesHG03111, HG02570, HG02450, HG02309, HG03419, NA19117, NA19474, HG03410
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645730
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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