A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453441



Internal ID21110994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123663501..123664900hg38UCSC Ensembl
chr9:126425780..126427179hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176554
Samples
Known GenesDENND1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453441
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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