A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189424



Internal ID20756464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35863826..35871371hg38UCSC Ensembl
chr9:35863823..35871368hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg387546
hg197546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450322
Supporting Variants
Samples
Known GenesLINC00950, OR13J1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189424
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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