A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536189



Internal ID20909544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50748304..50750911hg38UCSC Ensembl
chr1:51213976..51216583hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg382608
hg192608
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251625
Samples
Known GenesFAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536189
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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