A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv959446



Internal ID16253402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14541687..14566469hg38UCSC Ensembl
Innerchr3:14583194..14607976hg19UCSC Ensembl
Innerchr3:14558198..14582980hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3824783
hg1924783
hg1824783
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589774
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)nssv959446
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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