A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv959445



Internal ID16253401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14541479..14565193hg38UCSC Ensembl
Innerchr3:14582986..14606700hg19UCSC Ensembl
Innerchr3:14557990..14581704hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3823715
hg1923715
hg1823715
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589773
Supporting Variants
Samples
Known GenesGRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv959445
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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