A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155344



Internal ID20722384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18757944..18758473hg38UCSC Ensembl
chr7:18797567..18798096hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38530
hg19530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612588
Supporting Variants
Samples
Known GenesHDAC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155344
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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