A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17349696



Internal ID22575441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:238897550..238923333hg38UCSC Ensembl
chr1:239060850..239086633hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3825784
hg1925784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875588
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17349696
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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