A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288145



Internal ID20497363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61588982..61589042hg38UCSC Ensembl
chr1:62054654..62054714hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735074
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288145
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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