A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382386



Internal ID21039939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127969073..127998839hg38UCSC Ensembl
chr4:128890228..128919994hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3829767
hg1929767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110489
Samples
Known GenesC4orf29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382386
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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