A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569907



Internal ID20942978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139347338..139347796hg38UCSC Ensembl
chr7:139032084..139032542hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274418
Samples
Known GenesC7orf55-LUC7L2, LUC7L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569907
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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