A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601323



Internal ID16042046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29891740..29928644hg38UCSC Ensembl
Innerchr6:29859517..29896421hg19UCSC Ensembl
Innerchr6:29967496..30004400hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3836905
hg1936905
hg1836905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10348n54
Supporting Variantsnssv1051951, nssv1051953, nssv1051947, nssv1051952, nssv1051954, nssv1051945, nssv1051950, nssv1051949, nssv1051946, nssv1051956, nssv1051955, nssv1051948
Samples
Known GenesHCG4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601323
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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