A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382400



Internal ID21039953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43085710..43088964hg38UCSC Ensembl
chr5:43085812..43089066hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg383255
hg193255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130492
Samples
Known GenesLOC100506639
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382400
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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