A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388283



Internal ID21045836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82991601..82998300hg38UCSC Ensembl
chr4:83912754..83919453hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5348n223
Supporting Variantsnssv18119921
Samples
Known GenesLIN54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388283
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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