A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352483



Internal ID22578152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153668693..153668748hg38UCSC Ensembl
chr1:153641169..153641224hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872210
Supporting Variants
Samples
Known GenesILF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352483
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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