A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701446



Internal ID15438098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:166287594..166292886hg38UCSC Ensembl
Innerchr1:166256831..166262123hg19UCSC Ensembl
Innerchr1:164523455..164528747hg18UCSC Ensembl
Innerchr1:162988489..162993781hg17UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg385293
hg195293
hg185293
hg175293
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525333
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701446
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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