A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001163



Internal ID19090380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:115222929..115256030hg38UCSC Ensembl
Innerchr3:114941776..114974877hg19UCSC Ensembl
Innerchr3:116424466..116457567hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3833102
hg1933102
hg1833102
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604468
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)nsv1001163
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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