A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718103



Internal ID18669698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82172783..82314074hg38UCSC Ensembl
Innerchr15:82465124..82606410hg19UCSC Ensembl
Innerchr15:80252179..80393465hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38141292
hg19141287
hg18141287
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041040
Supporting Variants
Samples
Known GenesADAMTS7P1, EFTUD1, FAM154B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718103
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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