A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604142



Internal ID16391551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:92289835..92358587hg38UCSC Ensembl
Innerchr6:92999553..93068305hg19UCSC Ensembl
Innerchr6:93056274..93125026hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3868753
hg1968753
hg1868753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10839n54
Supporting Variantsnssv1068406
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604142
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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