A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565517



Internal ID20938588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116893262..116894190hg38UCSC Ensembl
chr7:116533316..116534244hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38929
hg19929
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272255
Samples
Known GenesCAPZA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565517
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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