A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064906



Internal ID20631946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89045866..89055922hg38UCSC Ensembl
chr1:89511549..89521605hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3810057
hg1910057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332370
Supporting Variants
Samples
Known GenesGBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064906
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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