A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522924



Internal ID15103531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:96765358..96790580hg38UCSC Ensembl
Innerchr15:97308588..97333810hg19UCSC Ensembl
Innerchr15:95109592..95134814hg18UCSC Ensembl
Innerchr15:95109592..95134814hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3825223
hg1925223
hg1825223
hg1725223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698585
Samples
Known GenesSPATA8, SPATA8-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522924
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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