A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009264



Internal ID19098482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145913953..145944673hg38UCSC Ensembl
Innerchr3:145631740..145662460hg19UCSC Ensembl
Innerchr3:147114430..147145150hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3830721
hg1930721
hg1830721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4917n100
Supporting Variantsnssv3606161
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)nsv1009264
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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