A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178649



Internal ID20745689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73047054..73047657hg38UCSC Ensembl
chr9:75661970..75662573hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437744
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178649
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00035


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