A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901161



Internal ID1586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24040905..24041285hg38UCSC Ensembl
chr1:24367395..24367775hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138468
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901161
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.015615


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