A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541168



Internal ID20914453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14943788..14948409hg38UCSC Ensembl
chr1:15270284..15274905hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg384622
hg194622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247500
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541168
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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