A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058389



Internal ID20625429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225914135..225927377hg38UCSC Ensembl
chr1:226101835..226115077hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg3813243
hg1913243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331294
Supporting Variants
Samples
Known GenesMIR6741, PYCR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058389
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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