A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195203



Internal ID20762243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28639480..28814968hg38UCSC Ensembl
chr9:28639478..28814966hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38175489
hg19175489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428337
Supporting Variants
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195203
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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