A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035969



Internal ID19125188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22385562..22736951hg38UCSC Ensembl
Innerchr15:23136152..23487534hg19UCSC Ensembl
Innerchr15:20687593..21038975hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38351390
hg19351383
hg18351383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3715543
Samples
Known GenesGOLGA8EP, GOLGA8I, HERC2P2, HERC2P7, WHAMMP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035969
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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