A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320177



Internal ID20853275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:208351603..208359579hg38UCSC Ensembl
chr1:208524948..208532924hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg387977
hg197977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199903
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320177
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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