A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553524



Internal ID20926634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46424240..46431404hg38UCSC Ensembl
chr2:46651379..46658543hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg387165
hg197165
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258018
Samples
Known GenesLOC101805491
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553524
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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