A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182619



Internal ID20749659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:609459..705232hg38UCSC Ensembl
chr9:609459..705232hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3895774
hg1995774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417030
Supporting Variants
Samples
Known GenesKANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182619
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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