A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546546



Internal ID20919762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150990380..150991503hg38UCSC Ensembl
chr1:150962856..150963979hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381124
hg191124
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248129
Samples
Known GenesANXA9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546546
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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