A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379124



Internal ID21036677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:114982077..115014555hg38UCSC Ensembl
chr4:115903233..115935711hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3832479
hg1932479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106455
Samples
Known GenesNDST4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379124
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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