A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608074



Internal ID16048797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:107538686..107620411hg38UCSC Ensembl
Innerchr7:107179131..107260856hg19UCSC Ensembl
Innerchr7:106966367..107048092hg18UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3881726
hg1981726
hg1881726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1092081
Samples
Known GenesBCAP29, COG5, DUS4L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608074
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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