A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607773



Internal ID16395182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89914999..90080467hg38UCSC Ensembl
Innerchr7:89544313..89709781hg19UCSC Ensembl
Innerchr7:89382249..89547717hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38165469
hg19165469
hg18165469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11496n54
Supporting Variantsnssv1155359
Samples1780854206_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607773
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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