A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528479



Internal ID15109086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:61215775..61221358hg38UCSC Ensembl
Innerchr2:61442910..61448493hg19UCSC Ensembl
Innerchr2:61296414..61301997hg18UCSC Ensembl
Innerchr2:61354561..61360144hg17UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg385584
hg195584
hg185584
hg175584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705082
Samples
Known GenesUSP34
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528479
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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