A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153596



Internal ID20720636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116113145..116113790hg38UCSC Ensembl
chr7:115753199..115753844hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38646
hg19646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602853
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153596
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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