A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620900



Internal ID7007770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83587291..83591608hg38UCSC Ensembl
Innerchr9:83587291..83591608hg38UCSC Ensembl
Outerchr9:83587170..83591741hg38UCSC Ensembl
chr9:86202206..86206523hg19UCSC Ensembl
Innerchr9:86202206..86206523hg19UCSC Ensembl
Outerchr9:86202085..86206656hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg384318
hg194318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13541138, essv13541137, essv13541139
SamplesHG00188, NA20800, HG00259
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620900
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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