A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189462



Internal ID20756502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38628239..38637213hg38UCSC Ensembl
chr9:38628236..38637210hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg388975
hg198975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442212
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189462
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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