A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011084



Internal ID19100301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52474..133665hg38UCSC Ensembl
Innerchr3:94157..175348hg19UCSC Ensembl
Innerchr3:69157..150348hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3881192
hg1981192
hg1881192
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4611n100
Supporting Variantsnssv3590260
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)nsv1011084
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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