A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011235



Internal ID19100452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:95151945..95519455hg38UCSC Ensembl
Innerchr3:94870789..95238299hg19UCSC Ensembl
Innerchr3:96353479..96720989hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38367511
hg19367511
hg18367511
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4815n100
Supporting Variantsnssv3603302
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)nsv1011235
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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