A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176553



Internal ID20743593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123660163..123779978hg38UCSC Ensembl
chr9:126422442..126542257hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38119816
hg19119816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445711
Supporting Variants
Samples
Known GenesDENND1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176553
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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