A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355538



Internal ID22581207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:238451507..238495564hg38UCSC Ensembl
chr1:238614807..238658864hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3844058
hg1944058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884633
Supporting Variants
Samples
Known GenesLINC01139
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355538
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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