A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152004



Internal ID15880703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100631901..100714131hg38UCSC Ensembl
Innerchr3:100350745..100432975hg19UCSC Ensembl
Innerchr3:101833435..101915665hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg3882231
hg1982231
hg1882231
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591162
Supporting Variants
SamplesNINDS_253
Known GenesGPR128, TFG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152004
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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