A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574986



Internal ID20948057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90602183..90642483hg38UCSC Ensembl
chr7:90231497..90271797hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3840301
hg1940301
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276882
Samples
Known GenesCDK14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574986
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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