A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998444



Internal ID19157980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26511964..26579428hg38UCSC Ensembl
Innerchr3:26553455..26620919hg19UCSC Ensembl
Innerchr3:26528459..26595923hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3867465
hg1967465
hg1867465
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4712n100
Supporting Variantsnssv3589556
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998444
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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