A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110444



Internal ID20677484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127422894..127428351hg38UCSC Ensembl
chr4:128344049..128349506hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg385458
hg195458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6393125
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110444
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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