A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535606



Internal ID20848709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63900787..63901950hg38UCSC Ensembl
chr2:64127921..64129084hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg381164
hg191164
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3907n223
Supporting Variantsnssv18260892
Samples
Known GenesVPS54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535606
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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