A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058053



Internal ID20625093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221688896..221689594hg38UCSC Ensembl
chr1:221862238..221862936hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38699
hg19699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330931
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058053
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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