A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151631



Internal ID20718671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133626406..133698118hg38UCSC Ensembl
chr7:133311159..133382871hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3871713
hg1971713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429455
Supporting Variants
Samples
Known GenesEXOC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151631
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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