A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151882



Internal ID15531489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14533936..14545810hg38UCSC Ensembl
Innerchr3:14575443..14587317hg19UCSC Ensembl
Innerchr3:14550447..14562321hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3811875
hg1911875
hg1811875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589772
Supporting Variants
SamplesHGDP01147
Known GenesGRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151882
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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