A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601318



Internal ID16042041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29891740..29925263hg38UCSC Ensembl
Innerchr6:29859517..29893040hg19UCSC Ensembl
Innerchr6:29967496..30001019hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3833524
hg1933524
hg1833524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10346n54
Supporting Variantsnssv1051936, nssv1051933, nssv1051935, nssv1051934, nssv1051937
Samples
Known GenesHCG4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601318
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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