A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384908



Internal ID21042461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143797106..144038018hg38UCSC Ensembl
chr4:144718259..144959171hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38240913
hg19240913
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213087
Samples
Known GenesGYPB, GYPE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384908
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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