A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061576



Internal ID20628616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46672666..46673047hg38UCSC Ensembl
chr1:47138338..47138719hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327951
Supporting Variants
Samples
Known GenesTEX38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061576
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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