A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556152



Internal ID20929223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149141064..149141480hg38UCSC Ensembl
chr7:148838156..148838572hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275230
Samples
Known GenesZNF398
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556152
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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