A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525157



Internal ID15452450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:43275338..43310870hg38UCSC Ensembl
Innerchr2:43502477..43538009hg19UCSC Ensembl
Innerchr2:43355981..43391513hg18UCSC Ensembl
Innerchr2:43414128..43449660hg17UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3835533
hg1935533
hg1835533
hg1735533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701230
Samples
Known GenesTHADA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525157
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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