A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171692



Internal ID20738732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102104104..102280460hg38UCSC Ensembl
chr9:104866386..105042742hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38176357
hg19176357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440673
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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