A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551205



Internal ID20924342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150223685..150224187hg38UCSC Ensembl
chr1:150196011..150196514hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg38503
hg19504
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247514
Samples
Known GenesANP32E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551205
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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