A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043615



Internal ID19132834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20376186..20538504hg38UCSC Ensembl
Innerchr15:20581439..20743782hg19UCSC Ensembl
Innerchr15:18841453..19003796hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38162319
hg19162344
hg18162344
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2243n100
Supporting Variantsnssv3535884, nssv3535886, nssv3535887, nssv3714559, nssv3535885, nssv3714558
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)nsv1043615
Frequency
Sample Size11257
Observed Gain5
Observed Loss1
Observed Complex0
Frequencyn/a


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