A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523274



Internal ID15450567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59679436..59681364hg38UCSC Ensembl
Innerchr15:59971635..59973563hg19UCSC Ensembl
Innerchr15:57758927..57760855hg18UCSC Ensembl
Innerchr15:57758927..57760855hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381929
hg191929
hg181929
hg171929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699008
Samples
Known GenesBNIP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523274
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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