A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559738



Internal ID20932809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74669412..74670507hg38UCSC Ensembl
chr7:74083737..74084832hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381096
hg191096
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276533
Samples
Known GenesGTF2I
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559738
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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