A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325153



Internal ID20858283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:30865070..30866292hg38UCSC Ensembl
chr1:31337917..31339139hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg381223
hg191223
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203572
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325153
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