A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162232



Internal ID20729272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95581788..95586720hg38UCSC Ensembl
chr7:95211100..95216032hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg384933
hg194933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602877
Supporting Variants
Samples
Known GenesPDK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162232
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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