A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397664



Internal ID21055217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:163792794..163843751hg38UCSC Ensembl
chr5:163219800..163270757hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3850958
hg1950958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128453
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397664
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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