A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411127



Internal ID21068680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148148601..148150100hg38UCSC Ensembl
chr5:147528164..147529663hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126738
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411127
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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