A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410222



Internal ID21067775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74500471..74509897hg38UCSC Ensembl
chr5:73796296..73805722hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg389427
hg199427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410222
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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