A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045735



Internal ID19134954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20368893..20538504hg38UCSC Ensembl
Innerchr15:20574146..20743782hg19UCSC Ensembl
Innerchr15:18834160..19003796hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38169612
hg19169637
hg18169637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2256n100
Supporting Variantsnssv3713809
Samples
Known GenesGOLGA6L6, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045735
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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