A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555709



Internal ID20928780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129735534..129736350hg38UCSC Ensembl
chr7:129375374..129376190hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271703
Samples
Known GenesNRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555709
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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