A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566434



Internal ID20939505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39418455..39419470hg38UCSC Ensembl
chr7:39458054..39459069hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381016
hg191016
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275657
Samples
Known GenesPOU6F2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566434
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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