A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005081



Internal ID19094298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:96560672..96599268hg38UCSC Ensembl
Innerchr3:96279516..96318112hg19UCSC Ensembl
Innerchr3:97762206..97800802hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3838597
hg1938597
hg1838597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4817n100
Supporting Variantsnssv3603306
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)nsv1005081
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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