A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325855



Internal ID20858987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51544991..51550578hg38UCSC Ensembl
chr1:52010663..52016250hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg385588
hg195588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061995
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325855
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