A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537017



Internal ID20910356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183257050..183257426hg38UCSC Ensembl
chr1:183226185..183226561hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249501
Samples
Known GenesNMNAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537017
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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