A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537764



Internal ID20911099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36052928..36053291hg38UCSC Ensembl
chr1:36518529..36518892hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251039
Samples
Known GenesAGO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537764
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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