A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901177



Internal ID1597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24176121..24179538hg38UCSC Ensembl
chr1:24502611..24506028hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383418
hg193418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424628
Supporting Variants
Samples
Known GenesIFNLR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901177
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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