A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322937



Internal ID20856052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145155701..145157400hg38UCSC Ensembl
chr1:149683923..149685617hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg381700
hg191695
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200784
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322937
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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