A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570008



Internal ID20943079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5176496..5878192hg38UCSC Ensembl
chr7:5216127..5917823hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38701697
hg19701697
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6546n223
Supporting Variantsnssv18274591
Samples
Known GenesACTB, FBXL18, FSCN1, MIR589, MIR6874, RNF216, RNF216-IT1, SLC29A4, TNRC18, WIPI2, ZNF815P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570008
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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