A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060573



Internal ID20627613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26217302..26221639hg38UCSC Ensembl
chr1:26543793..26548130hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg384338
hg194338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324578
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060573
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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