A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555412



Internal ID20928502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:233361716..233362228hg38UCSC Ensembl
chr2:234270362..234270874hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257370
Samples
Known GenesDGKD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555412
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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