A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703582



Internal ID15093548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75632102..75815389hg38UCSC Ensembl
Innerchr15:75924443..76107730hg19UCSC Ensembl
Innerchr15:73711498..73894785hg18UCSC Ensembl
Innerchr15:73711498..73894785hg17UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38183288
hg19183288
hg18183288
hg17183288
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527186
Supporting Variants
Samples
Known GenesCSPG4, DNM1P35, IMP3, MIR4313, ODF3L1, SNX33
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703582
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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