A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205102



Internal ID20772142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:81261881..81298917hg38UCSC Ensembl
chr1:81727566..81764602hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3837037
hg1937037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326246
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205102
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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