A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399500



Internal ID21057053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148362931..148370375hg38UCSC Ensembl
chr5:147742494..147749938hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg387445
hg197445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125931
Samples
Known GenesLOC102546294
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399500
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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