A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607660



Internal ID16395069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79014761..79036734hg38UCSC Ensembl
Innerchr7:78644077..78666050hg19UCSC Ensembl
Innerchr7:78482013..78503986hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3821974
hg1921974
hg1821974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1088521
Samples
Known GenesMAGI2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607660
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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