A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606280



Internal ID16393689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:14288341..14312376hg38UCSC Ensembl
Innerchr7:14327966..14352001hg19UCSC Ensembl
Innerchr7:14294491..14318526hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3824036
hg1924036
hg1824036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1079283
Samples
Known GenesDGKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606280
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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