A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323927



Internal ID20857050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94181002..94181566hg38UCSC Ensembl
chr1:94646558..94647122hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38565
hg19565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065608
Samples
Known GenesARHGAP29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323927
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