A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612406



Internal ID16399815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675712..136845084hg38UCSC Ensembl
Innerchr8:137687955..137857327hg19UCSC Ensembl
Innerchr8:137757137..137926509hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38169373
hg19169373
hg18169373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12343n54
Supporting Variantsnssv1122307, nssv1122315, nssv1122330, nssv1122317, nssv1122301, nssv1122337, nssv1122326, nssv1122324, nssv1122308, nssv1122310, nssv1122321, nssv1122338, nssv1122312, nssv1122325, nssv1122334, nssv1122335, nssv1122333, nssv1122313, nssv1122306, nssv1122302, nssv1122314, nssv1122318, nssv1122336, nssv1122331, nssv1122320, nssv1122332, nssv1122328, nssv1122309, nssv1122305, nssv1122316, nssv1122304, nssv1122329, nssv1122327, nssv1122323, nssv1122319, nssv1122311, nssv1122322, nssv1122303
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612406
Frequency
Sample Size17421
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


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