A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3593163



Internal ID6633443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161637723..161667370hg38UCSC Ensembl
Innerchr2:161637723..161667370hg38UCSC Ensembl
Outerchr2:161637223..161667870hg38UCSC Ensembl
chr2:162494233..162523880hg19UCSC Ensembl
Innerchr2:162494233..162523880hg19UCSC Ensembl
Outerchr2:162493733..162524380hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3829648
hg1929648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10740660, essv10740659
SamplesNA19355, HG03455
Known GenesSLC4A10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3593163
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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