A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626174



Internal ID15849707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43845453..43846176hg38UCSC Ensembl
Outerchr15:43828361..43855944hg38UCSC Ensembl
Innerchr15:44137651..44138374hg19UCSC Ensembl
Outerchr15:44120559..44148142hg19UCSC Ensembl
Innerchr15:41924943..41925666hg18UCSC Ensembl
Outerchr15:41907851..41935434hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3827584
hg1927584
hg1827584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511550
Supporting Variants
Samples1
Known GenesWDR76
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626174
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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