A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318094



Internal ID20851185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56951163..56952768hg38UCSC Ensembl
chr1:57416836..57418441hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg381606
hg191606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062382
Samples
Known GenesC8B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318094
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