A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007200



Internal ID18749731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62876175..63207417hg38UCSC Ensembl
Innerchr3:62861850..63193093hg19UCSC Ensembl
Innerchr3:62836890..63168133hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38331243
hg19331244
hg18331244
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3731137
Samples
Known GenesLINC00698
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007200
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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