A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377972



Internal ID21035525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43507101..43527300hg38UCSC Ensembl
chr5:43507203..43527402hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3820200
hg1920200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5739n223
Supporting Variantsnssv18214116
Samples
Known GenesC5orf34, PAIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377972
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer