A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606170



Internal ID16393579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:9718126..10008904hg38UCSC Ensembl
Innerchr7:9757755..10048531hg19UCSC Ensembl
Innerchr7:9724280..10015056hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38290779
hg19290777
hg18290777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155272
SamplesHGDP00151
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606170
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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