A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433628



Internal ID21091181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:141334592..141402343hg38UCSC Ensembl
chr8:142344691..142412443hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3867752
hg1967753
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234254
Samples
Known GenesGPR20, LOC731779
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433628
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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