A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376162



Internal ID21033715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39976323..40079750hg38UCSC Ensembl
chr4:39977943..40081370hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38103428
hg19103428
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5243n223
Supporting Variantsnssv18213599
Samples
Known GenesLOC344967, N4BP2, PDS5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376162
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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