A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523661



Internal ID15450954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:28992139..29015740hg38UCSC Ensembl
Innerchr2:29215005..29238606hg19UCSC Ensembl
Innerchr2:29068509..29092110hg18UCSC Ensembl
Innerchr2:29126656..29150257hg17UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg3823602
hg1923602
hg1823602
hg1723602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv213n21
Supporting Variantsnssv699462
Samples
Known GenesFAM179A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523661
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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