A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380821



Internal ID21038374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:92636417..92820757hg38UCSC Ensembl
chr4:93557568..93741908hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38184341
hg19184341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119725
Samples
Known GenesGRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380821
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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