A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18054105



Internal ID20621145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178957311..178978392hg38UCSC Ensembl
chr1:178926446..178947527hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3821082
hg1921082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318131
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18054105
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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