A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546083



Internal ID20919302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168950499..168950646hg38UCSC Ensembl
chr2:169807009..169807156hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256273
Samples
Known GenesABCB11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546083
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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