A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060596



Internal ID20627636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26568516..26569578hg38UCSC Ensembl
chr1:26895007..26896069hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381063
hg191063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319935
Supporting Variants
Samples
Known GenesRPS6KA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060596
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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