A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388405



Internal ID21045958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56645215..56648651hg38UCSC Ensembl
chr4:57511381..57514817hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg383437
hg193437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117898
Samples
Known GenesHOPX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388405
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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