A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606185



Internal ID16393594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:10126999..10165150hg38UCSC Ensembl
Innerchr7:10166626..10204777hg19UCSC Ensembl
Innerchr7:10133151..10171302hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3838152
hg1938152
hg1838152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11200n54
Supporting Variantsnssv1155281
SamplesHGDP01045
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606185
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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