A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381050



Internal ID21038603
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 StatusM
Merged Variants
Supporting Variantsnssv18210231
Samples
Known GenesKIAA1109
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381050
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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