A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607710



Internal ID16395119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:84508306..84539299hg38UCSC Ensembl
Innerchr7:84137622..84168615hg19UCSC Ensembl
Innerchr7:83975558..84006551hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3830994
hg1930994
hg1830994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1089371
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607710
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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