A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663338



Internal ID15053304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:75604810..75613058hg38UCSC Ensembl
Innerchr17:73600891..73609139hg19UCSC Ensembl
Innerchr17:71112486..71120734hg18UCSC Ensembl
Innerchr17:71112486..71120734hg17UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg388249
hg198249
hg188249
hg178249
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516133
Supporting Variants
Samples
Known GenesMYO15B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663338
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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