A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151586



Internal ID20718626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133320119..133329053hg38UCSC Ensembl
chr7:133004873..133013807hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg388935
hg198935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432055
Supporting Variants
Samples
Known GenesEXOC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151586
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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