A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389874



Internal ID21047427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37659805..37660435hg38UCSC Ensembl
chr4:37661427..37662057hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115974
Samples
Known GenesRELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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