A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155345



Internal ID20722385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18767320..18768049hg38UCSC Ensembl
chr7:18806943..18807672hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600593
Supporting Variants
Samples
Known GenesHDAC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155345
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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