A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601324



Internal ID16042047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29891740..29928882hg38UCSC Ensembl
Innerchr6:29859517..29896659hg19UCSC Ensembl
Innerchr6:29967496..30004638hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3837143
hg1937143
hg1837143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10348n54
Supporting Variantsnssv1051958, nssv1051957
Samples
Known GenesHCG4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601324
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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