A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324010



Internal ID20857133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59963150..60128959hg38UCSC Ensembl
chr1:60428822..60594631hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38165810
hg19165810
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202100
Samples
Known GenesC1orf87
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324010
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer