A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556011



Internal ID20929082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4687665..4688007hg38UCSC Ensembl
chr9:4687665..4688007hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280735
Samples
Known GenesCDC37L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556011
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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