A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564265



Internal ID20937336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6051656..6051954hg38UCSC Ensembl
chr7:6091287..6091585hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275439
Samples
Known GenesEIF2AK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564265
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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