A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671430



Internal ID15061396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100605598..100714131hg38UCSC Ensembl
Innerchr3:100324442..100432975hg19UCSC Ensembl
Innerchr3:101807132..101915665hg18UCSC Ensembl
Innerchr3:101807132..101915665hg17UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38108534
hg19108534
hg18108534
hg17108534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516418
Supporting Variants
Samples
Known GenesGPR128, TFG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671430
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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