A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157988



Internal ID20725028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66211257..66212563hg38UCSC Ensembl
chr7:65676244..65677550hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg381307
hg191307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608937
Supporting Variants
Samples
Known GenesTPST1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157988
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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