A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575018



Internal ID20948089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75754131..76110069hg38UCSC Ensembl
chr7:75383449..75739387hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38355939
hg19355939
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276561
Samples
Known GenesCCL24, CCL26, MDH2, MIR4651, POR, RHBDD2, SNORA14A, STYXL1, TMEM120A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575018
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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