A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701638



Internal ID15438290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75138185..75139454hg38UCSC Ensembl
Innerchr15:75430526..75431795hg19UCSC Ensembl
Innerchr15:73217579..73218848hg18UCSC Ensembl
Innerchr15:73217579..73218848hg17UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg381270
hg191270
hg181270
hg171270
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525506
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701638
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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