A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401083



Internal ID21058636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55119185..55119797hg38UCSC Ensembl
chr5:54415013..54415625hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131735
Samples
Known GenesCDC20B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401083
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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