A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3714808



Internal ID19013089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20406104..22033266hg38UCSC Ensembl
Innerchr15:20611357..22321217hg19UCSC Ensembl
Innerchr15:18871371..19822581hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381627163
hg191709861
hg18951211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049562
Supporting Variants
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, 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)nssv3714808
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer