A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401609



Internal ID21059162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119325163..119329711hg38UCSC Ensembl
chr5:118660858..118665406hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg384549
hg194549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126347
Samples
Known GenesTNFAIP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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