A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998459



Internal ID18811309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8470044..8507979hg38UCSC Ensembl
Innerchr3:8511730..8549665hg19UCSC Ensembl
Innerchr3:8486730..8524665hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3837936
hg1937936
hg1837936
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4677n100
Supporting Variantsnssv3591848, nssv3591849
Samples
Known GenesLMCD1, LMCD1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998459
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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