A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559377



Internal ID20932448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103151175..103151688hg38UCSC Ensembl
chr7:102791622..102792135hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7040n223
Supporting Variantsnssv18271598
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559377
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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