A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363598



Internal ID21021151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95743401..95770700hg38UCSC Ensembl
chr3:95462245..95489544hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3827300
hg1927300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4946n223
Supporting Variantsnssv18211245
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363598
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