A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3540868



Internal ID18839149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20441310..21078935hg38UCSC Ensembl
Innerchr15:20646563..21284264hg19UCSC Ensembl
Innerchr15:18906577..19548923hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38637626
hg19637702
hg18642347
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036082
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)nssv3540868
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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