A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360857



Internal ID22586526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:120409981..120410139hg38UCSC Ensembl
chr1:144588638..144588796hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878518
Supporting Variants
Samples
Known GenesLOC100288142
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360857
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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