A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705872



Internal ID15442524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:244313453..244328539hg38UCSC Ensembl
Innerchr1:244476755..244491841hg19UCSC Ensembl
Innerchr1:242543378..242558464hg18UCSC Ensembl
Innerchr1:240802796..240817882hg17UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3815087
hg1915087
hg1815087
hg1715087
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522504
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705872
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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