A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558271



Internal ID20931342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148751869..148752622hg38UCSC Ensembl
chr7:148448961..148449714hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275213
Samples
Known GenesCUL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558271
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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