A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541008



Internal ID20914293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156092601..156093079hg38UCSC Ensembl
chr1:156062392..156062870hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247149
Samples
Known GenesLMNA, MIR7851
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541008
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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