A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064402



Internal ID20631442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84113601..84114400hg38UCSC Ensembl
chr1:84579284..84580083hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333195
Supporting Variants
Samples
Known GenesPRKACB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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