A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320236



Internal ID20853334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32404245..32449317hg38UCSC Ensembl
chr1:32869846..32914918hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3845073
hg1945073
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203602
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320236
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