A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384077



Internal ID21041630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:92647125..92705228hg38UCSC Ensembl
chr4:93568276..93626379hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3858104
hg1958104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5367n223
Supporting Variantsnssv18119733
Samples
Known GenesGRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384077
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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