A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009455



Internal ID19098673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..55172hg38UCSC Ensembl
Innerchr3:60333..96855hg19UCSC Ensembl
Innerchr3:35333..71855hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3836518
hg1936523
hg1836523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4602n100
Supporting Variantsnssv3593505, nssv3593504, nssv3593503
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)nsv1009455
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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