A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052446



Internal ID20619486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160163431..160164617hg38UCSC Ensembl
chr1:160133221..160134407hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg381187
hg191187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332667
Supporting Variants
Samples
Known GenesATP1A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052446
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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