A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008016



Internal ID20575056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:21673501..21674000hg38UCSC Ensembl
chr13:22247640..22248139hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477173
Supporting Variants
Samples
Known GenesFGF9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008016
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.08336


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