A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388729



Internal ID21046282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17646506..17776564hg38UCSC Ensembl
chr5:17646615..17776673hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38130059
hg19130059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5675n223
Supporting Variantsnssv18128580
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388729
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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