A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606906



Internal ID16394315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:50605969..50626760hg38UCSC Ensembl
Innerchr7:50673666..50694457hg19UCSC Ensembl
Innerchr7:50641160..50661951hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3820792
hg1920792
hg1820792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1083848
Samples
Known GenesGRB10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606906
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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