A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391379



Internal ID21048932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:92481698..92502930hg38UCSC Ensembl
chr4:93402849..93424081hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3821233
hg1921233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120749
Samples
Known GenesGRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391379
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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