A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434453



Internal ID22492323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123854601..123855353hg38UCSC Ensembl
chr9:126616880..126617632hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921912
Supporting Variants
Samples
Known GenesDENND1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434453
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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