A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052174



Internal ID19141393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85798051..85813084hg38UCSC Ensembl
Innerchr15:86341282..86356315hg19UCSC Ensembl
Innerchr15:84142286..84157319hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3815034
hg1915034
hg1815034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2653n100
Supporting Variantsnssv3555092, nssv3555093
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052174
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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