A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606184



Internal ID16393593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:10123160..10171980hg38UCSC Ensembl
Innerchr7:10162787..10211607hg19UCSC Ensembl
Innerchr7:10129312..10178132hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3848821
hg1948821
hg1848821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11200n54
Supporting Variantsnssv1155280
SamplesHGDP01041
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606184
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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