A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18148417



Internal ID20715457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101599156..101605768hg38UCSC Ensembl
chr7:101242436..101249048hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg386613
hg196613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608506
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18148417
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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