A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522621



Internal ID15449914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:154591203..154602534hg38UCSC Ensembl
Innerchr2:155447715..155459046hg19UCSC Ensembl
Innerchr2:155155961..155167292hg18UCSC Ensembl
Innerchr2:155273223..155284554hg17UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3811332
hg1911332
hg1811332
hg1711332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706017
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522621
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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