A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610156



Internal ID16397565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8305721..8349823hg38UCSC Ensembl
Innerchr8:8163243..8207339hg19UCSC Ensembl
Innerchr8:8200653..8244749hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3844103
hg1944097
hg1844097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156575
Samples1780862275_A
Known GenesSGK223
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610156
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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