A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011155



Internal ID18753689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:184843753..184899600hg38UCSC Ensembl
Innerchr3:184561541..184617388hg19UCSC Ensembl
Innerchr3:186044235..186100082hg18UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3855848
hg1955848
hg1855848
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3615007
Samples
Known GenesVPS8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011155
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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