A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386808



Internal ID21044361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147762603..147781719hg38UCSC Ensembl
chr4:148683754..148702870hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3819117
hg1919117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18109616
Samples
Known GenesARHGAP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386808
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