A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547991



Internal ID20921190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203386486..203387418hg38UCSC Ensembl
chr1:203355614..203356546hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38933
hg19933
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547991
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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