A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561505



Internal ID20934576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116914740..116914998hg38UCSC Ensembl
chr7:116554794..116555052hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272257
Samples
Known GenesCAPZA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561505
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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