A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389551



Internal ID21047104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120471973..120494470hg38UCSC Ensembl
chr4:121393128..121415625hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3822498
hg1922498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105885
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389551
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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