A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002577



Internal ID18745109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..93308hg38UCSC Ensembl
Innerchr3:60333..134991hg19UCSC Ensembl
Innerchr3:35333..109991hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3874654
hg1974659
hg1874659
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4605n100
Supporting Variantsnssv3593528
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)nsv1002577
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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