A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702292



Internal ID15092258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71861659..71925695hg38UCSC Ensembl
Innerchr15:72154000..72218036hg19UCSC Ensembl
Innerchr15:69941054..70005090hg18UCSC Ensembl
Innerchr15:69941054..70005090hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3864037
hg1964037
hg1864037
hg1764037
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)nssv702292
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer