A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064207



Internal ID20631247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8122301..8132400hg38UCSC Ensembl
chr1:8182361..8192460hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3810100
hg1910100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326426
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064207
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00764


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