A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395123



Internal ID21052676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:36179001..36179800hg38UCSC Ensembl
chr5:36179103..36179902hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130439
Samples
Known GenesSKP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395123
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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