A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423267



Internal ID21080820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140419094..141917651hg38UCSC Ensembl
chr8:141429193..142999012hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg381498558
hg191569820
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231675
Samples
Known GenesAGO2, CHRAC1, DENND3, GPR20, LOC731779, MROH5, PTK2, PTP4A3, SLC45A4, TRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423267
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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