A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564239



Internal ID20937310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92330821..92331494hg38UCSC Ensembl
chr7:91960135..91960808hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38674
hg19674
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276922
Samples
Known GenesANKIB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564239
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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