A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3715855



Internal ID19014136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20056971..20609659hg38UCSC Ensembl
Innerchr15:20262224..20814965hg19UCSC Ensembl
Innerchr15:18522238..19074979hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38552689
hg19552742
hg18552742
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044097
Supporting Variants
Samples
Known GenesCHEK2P2, GOLGA6L6, GOLGA8CP, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3715855
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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