A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604597



Internal ID16392006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:124332380..124366327hg38UCSC Ensembl
Innerchr6:124653526..124687473hg19UCSC Ensembl
Innerchr6:124695225..124729172hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3833948
hg1933948
hg1833948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1072395
Samples
Known GenesNKAIN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604597
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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