A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442943



Internal ID21100496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100130101..100131700hg38UCSC Ensembl
chr9:102892383..102893982hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171531
Samples
Known GenesINVS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442943
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