A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042089



Internal ID19131308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76562757..76723786hg38UCSC Ensembl
Innerchr15:76855098..77016127hg19UCSC Ensembl
Innerchr15:74642153..74803182hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38161030
hg19161030
hg18161030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553744
Samples
Known GenesSCAPER
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042089
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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