A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368644



Internal ID21026197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:76105982..76277915hg38UCSC Ensembl
chr3:76155133..76327066hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38171934
hg19171934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102431
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368644
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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