A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321793



Internal ID20854901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156110680..156111323hg38UCSC Ensembl
chr1:156080471..156081114hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200920
Samples
Known GenesLMNA, MIR7851
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321793
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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