A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606905



Internal ID16047628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:50476365..50498265hg38UCSC Ensembl
Innerchr7:50544063..50565963hg19UCSC Ensembl
Innerchr7:50511557..50533457hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3821901
hg1921901
hg1821901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1083847
Samples
Known GenesDDC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606905
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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