A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540446



Internal ID20913738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15839414..15839818hg38UCSC Ensembl
chr1:16165909..16166313hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247776
Samples
Known GenesFLJ37453
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540446
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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