A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037180



Internal ID19126399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20240873..20781357hg38UCSC Ensembl
Innerchr15:20446126..20986686hg19UCSC Ensembl
Innerchr15:18706140..19246735hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38540485
hg19540561
hg18540596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2211n100
Supporting Variantsnssv3534730
Samples
Known GenesCHEK2P2, 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)nsv1037180
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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