A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320559



Internal ID20853658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234698701..234830400hg38UCSC Ensembl
chr1:234834448..234966147hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38131700
hg19131700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv556n223
Supporting Variantsnssv18202397
Samples
Known GenesLINC01132
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320559
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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