A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694196



Internal ID15430848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24861936..24862075hg38UCSC Ensembl
Innerchr15:25107083..25107222hg19UCSC Ensembl
Innerchr15:22658176..22658315hg18UCSC Ensembl
Innerchr15:22658176..22658315hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38140
hg19140
hg18140
hg17140
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516596
Supporting Variants
Samples
Known GenesSNRPN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694196
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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