A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565501



Internal ID20938572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139134455..139135104hg38UCSC Ensembl
chr7:138819201..138819850hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7132n223
Supporting Variantsnssv18274406
Samples
Known GenesTTC26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565501
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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