A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539580



Internal ID20912876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:164580101..164580488hg38UCSC Ensembl
chr2:165436611..165436998hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255817
Samples
Known GenesGRB14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539580
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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