A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009618



Internal ID18752149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155652245..155774388hg38UCSC Ensembl
Innerchr3:155370034..155492177hg19UCSC Ensembl
Innerchr3:156852728..156974871hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38122144
hg19122144
hg18122144
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606354
Samples
Known GenesC3orf33, PLCH1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009618
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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