A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007679



Internal ID19096898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35448384..35545762hg38UCSC Ensembl
Innerchr3:35489876..35587254hg19UCSC Ensembl
Innerchr3:35464880..35562258hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3897379
hg1997379
hg1897379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4716n100
Supporting Variantsnssv3589597
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)nsv1007679
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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