A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892871



Internal ID19183691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:83736956..84158440hg38UCSC Ensembl
Outerchr2:83736956..84158440hg38UCSC Ensembl
Innerchr2:83964080..84385564hg19UCSC Ensembl
Outerchr2:83964080..84385564hg19UCSC Ensembl
Innerchr2:83817591..84239075hg18UCSC Ensembl
Outerchr2:83817591..84239075hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38421485
hg19421485
hg18421485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798255
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892871
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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