A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694825



Internal ID15084791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71846137..71891773hg38UCSC Ensembl
Innerchr15:72138478..72184114hg19UCSC Ensembl
Innerchr15:69925532..69971168hg18UCSC Ensembl
Innerchr15:69925532..69971168hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3845637
hg1945637
hg1845637
hg1745637
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
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)nssv694825
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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