A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544567



Internal ID20917806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212998141..212998622hg38UCSC Ensembl
chr1:213171483..213171964hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248539
Samples
Known GenesANGEL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544567
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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