A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013248



Internal ID19102466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:84668760..84725599hg38UCSC Ensembl
Innerchr3:84717911..84774750hg19UCSC Ensembl
Innerchr3:84800601..84857440hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3856840
hg1956840
hg1856840
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4803n100
Supporting Variantsnssv3596263
Samples
Known GenesLINC00971
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013248
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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