A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18119765



Internal ID20686805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:92835298..92835665hg38UCSC Ensembl
chr4:93756449..93756816hg19UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390644
Supporting Variants
Samples
Known GenesGRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18119765
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0017


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