A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176435



Internal ID20743475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137626155..137629719hg38UCSC Ensembl
chr9:140520607..140524171hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg383565
hg193565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445643
Supporting Variants
Samples
Known GenesEHMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176435
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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