A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv967561



Internal ID16261517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89244999..89343628hg38UCSC Ensembl
Innerchr3:89294149..89392778hg19UCSC Ensembl
Innerchr3:89376839..89475468hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3898630
hg1998630
hg1898630
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590921
Supporting Variants
Samples
Known GenesEPHA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv967561
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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