A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537202



Internal ID20910541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:193099336..193100496hg38UCSC Ensembl
chr1:193068466..193069626hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg381161
hg191161
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250245
Samples
Known GenesGLRX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537202
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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