A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705205



Internal ID15441857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9919583..9921262hg38UCSC Ensembl
Innerchr5:9919695..9921374hg19UCSC Ensembl
Innerchr5:9972695..9974374hg18UCSC Ensembl
Innerchr5:9972695..9974374hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381680
hg191680
hg181680
hg171680
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517239
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705205
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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