A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065245



Internal ID20632285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95743961..95744689hg38UCSC Ensembl
chr1:96209517..96210245hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333270
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065245
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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