A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007403



Internal ID19096622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:186669016..186709255hg38UCSC Ensembl
Innerchr3:186386805..186427044hg19UCSC Ensembl
Innerchr3:187869499..187909738hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3840240
hg1940240
hg1840240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5003n100
Supporting Variantsnssv3615018
Samples
Known GenesHRG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007403
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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