A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415196



Internal ID21072749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:92069105..92349850hg38UCSC Ensembl
chr5:91364922..91636128hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38280746
hg19271207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135592
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415196
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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