A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718126



Internal ID18669721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84192647..84554155hg38UCSC Ensembl
Innerchr15:84861399..85097386hg19UCSC Ensembl
Innerchr15:82652403..82898390hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38361509
hg19235988
hg18245988
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045761
Supporting Variants
Samples
Known GenesDNM1P41, GOLGA6L4, GOLGA6L5P, LOC388152, LOC440300, LOC642423, UBE2Q2P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718126
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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