A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003543



Internal ID19092761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:116377351..116392583hg38UCSC Ensembl
Innerchr3:116096198..116111430hg19UCSC Ensembl
Innerchr3:117578888..117594120hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3815233
hg1915233
hg1815233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4842n100
Supporting Variantsnssv3604473
Samples
Known GenesLSAMP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003543
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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