A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3735184



Internal ID18686779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98565439..98662629hg38UCSC Ensembl
Innerchr3:98284283..98381473hg19UCSC Ensembl
Innerchr3:99766973..99864163hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3897191
hg1997191
hg1897191
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000357
Supporting Variants
Samples
Known GenesCPOX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3735184
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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