A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620845



Internal ID7007715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80200781..80204290hg38UCSC Ensembl
Innerchr9:80200781..80204290hg38UCSC Ensembl
Outerchr9:80200496..80204619hg38UCSC Ensembl
chr9:82815696..82819205hg19UCSC Ensembl
Innerchr9:82815696..82819205hg19UCSC Ensembl
Outerchr9:82815411..82819534hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg383510
hg193510
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13535257, essv13535258
SamplesHG00256, HG00371
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620845
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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