A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447636



Internal ID21105189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34414093..34545288hg38UCSC Ensembl
chr9:34414091..34545286hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38131196
hg19131196
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233940
Samples
Known GenesDNAI1, ENHO, FAM219A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447636
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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