A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv975218



Internal ID16269174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:142500700..142589228hg38UCSC Ensembl
Innerchr3:142219542..142308070hg19UCSC Ensembl
Innerchr3:143702232..143790760hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3888529
hg1988529
hg1888529
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591919
Supporting Variants
Samples
Known GenesATR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv975218
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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