A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713723



Internal ID19012004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20327352..20996195hg38UCSC Ensembl
Innerchr15:20532605..21201524hg19UCSC Ensembl
Innerchr15:18792619..19466183hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38668844
hg19668920
hg18673565
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047800
Supporting Variants
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713723
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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