A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569362



Internal ID20942433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116793354..116793662hg38UCSC Ensembl
chr7:116433408..116433716hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272250
Samples
Known GenesMET
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569362
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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