A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698864



Internal ID15435516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:226047182..226052129hg38UCSC Ensembl
Innerchr1:226234883..226239830hg19UCSC Ensembl
Innerchr1:224301506..224306453hg18UCSC Ensembl
Innerchr1:222541618..222546565hg17UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg384948
hg194948
hg184948
hg174948
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523155
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698864
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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