A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022404



Internal ID22084035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:134633220..134640762hg38UCSC Ensembl
Outerchr7:134627769..134641192hg38UCSC Ensembl
Innerchr7:134317972..134325514hg19UCSC Ensembl
Outerchr7:134312521..134325944hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3813424
hg1913424
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156728
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022404
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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