A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019191



Internal ID18761725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:159134068..159622215hg38UCSC Ensembl
Innerchr6:159555100..160043247hg19UCSC Ensembl
Innerchr6:159475088..159963237hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38488148
hg19488148
hg18488150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654491, nssv3654490
Samples
Known GenesFNDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019191
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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