A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380655



Internal ID21038208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69936501..69937200hg38UCSC Ensembl
chr4:70802219..70802918hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119046
Samples
Known GenesCSN1S1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380655
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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