A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395817



Internal ID21053370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:110993564..111020994hg38UCSC Ensembl
chr5:110329263..110356693hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3827431
hg1927431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124946
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395817
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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