A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032032



Internal ID19121254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:133142676..133168229hg38UCSC Ensembl
Innerchr8:134154920..134180473hg19UCSC Ensembl
Innerchr8:134224102..134249655hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3825554
hg1925554
hg1825554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691575
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)nsv1032032
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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