A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571581



Internal ID20944652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99253222..99254433hg38UCSC Ensembl
chr7:98850845..98852056hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381212
hg191212
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275852
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571581
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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