A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218802



Internal ID20785842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2697221..2797403hg38UCSC Ensembl
chr9:2697221..2797403hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38100183
hg19100183
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416196
Supporting Variants
Samples
Known GenesKCNV2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218802
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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