A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210231



Internal ID20777271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122024200..122297002hg38UCSC Ensembl
chr4:122945355..123218157hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38272803
hg19272803
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381050
Supporting Variants
Samples
Known GenesKIAA1109
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210231
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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