A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18056844



Internal ID20623885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:198910908..198911537hg38UCSC Ensembl
chr1:198880037..198880666hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322652
Supporting Variants
Samples
Known GenesMIR181A1HG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18056844
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00043


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