A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549253



Internal ID20922421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15844563..15845693hg38UCSC Ensembl
chr1:16171058..16172188hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg381131
hg191131
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247778
Samples
Known GenesFLJ37453
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549253
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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