A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572552



Internal ID20945623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28539300..28547115hg38UCSC Ensembl
chr7:28578918..28586733hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg387816
hg197816
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273429
Samples
Known GenesCREB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572552
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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