A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000608



Internal ID19089825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..84526hg38UCSC Ensembl
Innerchr3:60333..126209hg19UCSC Ensembl
Innerchr3:35333..101209hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3865872
hg1965877
hg1865877
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4604n100
Supporting Variantsnssv3593526
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)nsv1000608
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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