A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700310



Internal ID15090276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:153796506..153800764hg38UCSC Ensembl
Innerchr1:153768982..153773240hg19UCSC Ensembl
Innerchr1:152035606..152039864hg18UCSC Ensembl
Innerchr1:150582055..150586313hg17UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg384259
hg194259
hg184259
hg174259
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515962
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700310
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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