A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402231



Internal ID22460101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:99917990..99918116hg38UCSC Ensembl
chr1:100383546..100383672hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877200
Supporting Variants
Samples
Known GenesAGL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402231
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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