A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383514



Internal ID21041067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99935418..99935887hg38UCSC Ensembl
chr4:100856575..100857044hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121360
Samples
Known GenesDNAJB14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383514
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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