A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612421



Internal ID16399830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675987..136839412hg38UCSC Ensembl
Innerchr8:137688230..137851655hg19UCSC Ensembl
Innerchr8:137757412..137920837hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38163426
hg19163426
hg18163426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12343n54
Supporting Variantsnssv1156191, nssv1156192, nssv1122397, nssv1156193
Samples1798860361_A, 1780854129_A, HGDP01386
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612421
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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