A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538362



Internal ID20911679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:127992139..127994360hg38UCSC Ensembl
chr2:128749713..128751934hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg382222
hg192222
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256795
Samples
Known GenesSAP130
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538362
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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