A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151582



Internal ID20718622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133267355..133673555hg38UCSC Ensembl
chr7:132952110..133358308hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38406201
hg19406199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429045
Supporting Variants
Samples
Known GenesEXOC4, MIR6133
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151582
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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