A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382150



Internal ID21039703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:110058740..110059554hg38UCSC Ensembl
chr4:110979896..110980710hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38815
hg19815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107792
Samples
Known GenesELOVL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382150
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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