A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037177



Internal ID19126396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20327352..20828228hg38UCSC Ensembl
Innerchr15:20532605..21033557hg19UCSC Ensembl
Innerchr15:18792619..19293609hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38500877
hg19500953
hg18500991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2245n100
Supporting Variantsnssv3713722
Samples
Known GenesCXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037177
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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