A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397777



Internal ID21055330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:63292328..63301664hg38UCSC Ensembl
chr5:62588155..62597491hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg389337
hg199337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132557
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397777
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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