A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450604



Internal ID21108157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99993337..100281630hg38UCSC Ensembl
chr9:102755619..103043912hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38288294
hg19288294
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229040
Samples
Known GenesERP44, INVS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450604
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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