A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034894



Internal ID18777426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:143827429..143848899hg38UCSC Ensembl
Innerchr6:144148566..144170036hg19UCSC Ensembl
Innerchr6:144190259..144211729hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3821471
hg1921471
hg1821471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654454
Samples
Known GenesLTV1, PHACTR2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034894
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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