A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702068



Internal ID15438720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84921267..84956998hg38UCSC Ensembl
Innerchr15:85464498..85500229hg19UCSC Ensembl
Innerchr15:83265502..83301233hg18UCSC Ensembl
Innerchr15:83265502..83301233hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3835732
hg1935732
hg1835732
hg1735732
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525868
Supporting Variants
Samples
Known GenesSLC28A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702068
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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