A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064974



Internal ID20632014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9033130..9039404hg38UCSC Ensembl
chr1:9093189..9099463hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg386275
hg196275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332475
Supporting Variants
Samples
Known GenesSLC2A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064974
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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