A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566067



Internal ID20939138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139134408..139135099hg38UCSC Ensembl
chr7:138819154..138819845hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38692
hg19692
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7132n223
Supporting Variantsnssv18274405
Samples
Known GenesTTC26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566067
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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