A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18158096



Internal ID20725136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67820704..67827171hg38UCSC Ensembl
chr7:67285691..67292158hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg386468
hg196468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601162
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18158096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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