A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402196



Internal ID21059749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:86334327..86342108hg38UCSC Ensembl
chr5:85630145..85637926hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg387782
hg197782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135997
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402196
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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