A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176543



Internal ID20743583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123398648..123400795hg38UCSC Ensembl
chr9:126160927..126163074hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg382148
hg192148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449830
Supporting Variants
Samples
Known GenesDENND1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176543
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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