A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325685



Internal ID20858816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154181754..154189040hg38UCSC Ensembl
chr1:154154230..154161516hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg387287
hg197287
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200499
Samples
Known GenesTPM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325685
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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