A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013694



Internal ID19102913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41529109..41911840hg38UCSC Ensembl
Innerchr3:41570600..41953332hg19UCSC Ensembl
Innerchr3:41545604..41928336hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38382732
hg19382733
hg18382733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4724n100
Supporting Variantsnssv3589709
Samples
Known GenesULK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013694
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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