A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698574



Internal ID15088540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248159177..248179535hg38UCSC Ensembl
Innerchr1:248322479..248342837hg19UCSC Ensembl
Innerchr1:246389102..246409460hg18UCSC Ensembl
Innerchr1:244648520..244668878hg17UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3820359
hg1920359
hg1820359
hg1720359
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515858
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698574
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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