A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445194



Internal ID21102747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116426209..116521654hg38UCSC Ensembl
chr9:119188488..119283933hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3895446
hg1995446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174123
Samples
Known GenesASTN2, LOC100128505
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445194
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