A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156896



Internal ID15509073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:141423771..141451594hg38UCSC Ensembl
Innerchr8:142433871..142461694hg19UCSC Ensembl
Innerchr8:142503053..142530876hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3827824
hg1927824
hg1827824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612581
Supporting Variants
Samples1782681313_A
Known GenesMROH5, PTP4A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156896
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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