A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400856



Internal ID21058409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:118703691..118750984hg38UCSC Ensembl
chr5:118039386..118086679hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3847294
hg1947294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123572
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400856
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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