A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436781



Internal ID21094334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97037034..97043313hg38UCSC Ensembl
chr9:99799316..99805595hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg386280
hg196280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190020
Samples
Known GenesCTSV
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436781
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