A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522771



Internal ID15450064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:53466481..53474186hg38UCSC Ensembl
Innerchr2:53693619..53701324hg19UCSC Ensembl
Innerchr2:53547123..53554828hg18UCSC Ensembl
Innerchr2:53605270..53612975hg17UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg387706
hg197706
hg187706
hg177706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698412
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522771
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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