A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010627



Internal ID19099844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..74907hg38UCSC Ensembl
Innerchr3:60333..116590hg19UCSC Ensembl
Innerchr3:35333..91590hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3856253
hg1956258
hg1856258
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4604n100
Supporting Variantsnssv3593521, nssv3593522
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)nsv1010627
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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