A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705758



Internal ID15442410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:166287594..166295006hg38UCSC Ensembl
Innerchr1:166256831..166264243hg19UCSC Ensembl
Innerchr1:164523455..164530867hg18UCSC Ensembl
Innerchr1:162988489..162995901hg17UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg387413
hg197413
hg187413
hg177413
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv529043
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705758
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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