A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021793



Internal ID22083424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156089623..156094352hg38UCSC Ensembl
Outerchr7:156087157..156095374hg38UCSC Ensembl
Innerchr7:155882317..155887046hg19UCSC Ensembl
Outerchr7:155879851..155888068hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg388218
hg198218
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156765
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021793
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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