A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429396



Internal ID21086949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2811903..2816517hg38UCSC Ensembl
chr9:2811903..2816517hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg384615
hg194615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182111
Samples
Known GenesKIAA0020
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429396
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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