A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322355



Internal ID20855467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52167115..52179294hg38UCSC Ensembl
chr1:52632787..52644966hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3812180
hg1912180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062029
Samples
Known GenesZFYVE9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322355
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