A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380680



Internal ID21038233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:24201201..24203000hg38UCSC Ensembl
chr5:24201310..24203109hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129056
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380680
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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