A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154796



Internal ID20721836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18166201..18350900hg38UCSC Ensembl
chr7:18205824..18390523hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38184700
hg19184700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606923
Supporting Variants
Samples
Known GenesHDAC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154796
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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