A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696349



Internal ID15086315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71861659..72033254hg38UCSC Ensembl
Innerchr15:72154000..72325595hg19UCSC Ensembl
Innerchr15:69941054..70112649hg18UCSC Ensembl
Innerchr15:69941054..70112649hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38171596
hg19171596
hg18171596
hg17171596
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516871
Supporting Variants
Samples
Known GenesMYO9A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696349
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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