A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540499



Internal ID20913792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61720299..61721566hg38UCSC Ensembl
chr1:62185971..62187238hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381268
hg191268
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250479
Samples
Known GenesTM2D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540499
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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