A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154797



Internal ID20721837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18185136..18317655hg38UCSC Ensembl
chr7:18224759..18357278hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38132520
hg19132520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602243
Supporting Variants
Samples
Known GenesHDAC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154797
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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