A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229040



Internal ID20796080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99993337..100281630hg38UCSC Ensembl
chr9:102755619..103043912hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38288294
hg19288294
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450604
Supporting Variants
Samples
Known GenesERP44, INVS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229040
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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