A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438161



Internal ID21095714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34416743..34420243hg38UCSC Ensembl
chr9:34416741..34420241hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg383501
hg193501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190591
Samples
Known GenesFAM219A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438161
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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