A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327919



Internal ID20861063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:197852608..197914971hg38UCSC Ensembl
chr1:197821738..197884101hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3862364
hg1962364
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202319
Samples
Known GenesC1orf53, LHX9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327919
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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