A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176436



Internal ID20743476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137643301..137647800hg38UCSC Ensembl
chr9:140537753..140542252hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439843
Supporting Variants
Samples
Known GenesEHMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176436
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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