A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177331



Internal ID20744371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88359515..88361378hg38UCSC Ensembl
chr9:90974430..90976293hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg381864
hg191864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455022
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177331
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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