A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555946



Internal ID20929017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132328448..132330002hg38UCSC Ensembl
chr3:132047292..132048846hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381555
hg191555
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260253
Samples
Known GenesACPP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555946
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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