A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416272



Internal ID21073825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56142401..56186000hg38UCSC Ensembl
chr8:57054960..57098559hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3843600
hg1943600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7356n223
Supporting Variantsnssv18218700
Samples
Known GenesPLAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416272
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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