A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561161



Internal ID20934232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26802456..26802858hg38UCSC Ensembl
chr7:26842075..26842477hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273376
Samples
Known GenesSKAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561161
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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