A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384537



Internal ID21042090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42423601..42424100hg38UCSC Ensembl
chr5:42423703..42424202hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130449
Samples
Known GenesGHR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384537
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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