A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547255



Internal ID20920457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37169530..37170501hg38UCSC Ensembl
chr2:37396673..37397644hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38972
hg19972
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260183
Samples
Known GenesSULT6B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547255
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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