A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398400



Internal ID21055953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51469855..51473229hg38UCSC Ensembl
chr5:50765689..50769063hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg383375
hg193375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131268
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398400
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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