A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601208



Internal ID16041931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27842848..28001226hg38UCSC Ensembl
Innerchr6:27810626..27969004hg19UCSC Ensembl
Innerchr6:27918605..28076983hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38158379
hg19158379
hg18158379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1051654
Samples
Known GenesHIST1H1B, HIST1H2AL, HIST1H2AM, HIST1H2BO, HIST1H3I, HIST1H3J, HIST1H4L, OR2B2, OR2B6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601208
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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