A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18109489



Internal ID20676529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146267291..146267680hg38UCSC Ensembl
chr4:147188443..147188832hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391904
Supporting Variants
Samples
Known GenesSLC10A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18109489
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00045


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