A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705776



Internal ID15442428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26623563..26704720hg38UCSC Ensembl
Innerchr4:26625185..26706342hg19UCSC Ensembl
Innerchr4:26234283..26315440hg18UCSC Ensembl
Innerchr4:26301454..26382611hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3881158
hg1981158
hg1881158
hg1781158
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522423
Supporting Variants
Samples
Known GenesTBC1D19
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705776
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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