A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437829



Internal ID21095382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123913683..123919667hg38UCSC Ensembl
chr9:126675962..126681946hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385985
hg195985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7932n223
Supporting Variantsnssv18176575
Samples
Known GenesDENND1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437829
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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