A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318563



Internal ID20851655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56796507..56797364hg38UCSC Ensembl
chr1:57262180..57263037hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38858
hg19858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061751
Samples
Known GenesC1orf168
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318563
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