A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064822



Internal ID20631862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85654920..85655694hg38UCSC Ensembl
chr1:86120603..86121377hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332900
Supporting Variants
Samples
Known GenesZNHIT6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064822
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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