A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443317



Internal ID21100870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93352601..93362800hg38UCSC Ensembl
chr9:96114883..96125082hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3810200
hg1910200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7879n223
Supporting Variantsnssv18183465
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443317
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