A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569145



Internal ID20942216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26444169..26445911hg38UCSC Ensembl
chr7:26483789..26485531hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg381743
hg191743
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6626n223
Supporting Variantsnssv18273368
Samples
Known GenesLOC441204
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569145
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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