A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546794



Internal ID20920004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:114517447..114518362hg38UCSC Ensembl
chr2:115275024..115275939hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38916
hg19916
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256569
Samples
Known GenesDPP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546794
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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