A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205201



Internal ID20772241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8840894..8876597hg38UCSC Ensembl
chr1:8900953..8936656hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3835704
hg1935704
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324723
Supporting Variants
Samples
Known GenesENO1, MIR6728
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205201
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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