A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542646



Internal ID20915904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63900758..63901743hg38UCSC Ensembl
chr2:64127892..64128877hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38986
hg19986
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3907n223
Supporting Variantsnssv18258760
Samples
Known GenesVPS54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542646
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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