A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18106459



Internal ID20673499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:115000479..115001225hg38UCSC Ensembl
chr4:115921635..115922381hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391797
Supporting Variants
Samples
Known GenesNDST4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18106459
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0005


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