A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571959



Internal ID20945030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98218783..98219585hg38UCSC Ensembl
chr8:99231011..99231813hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38803
hg19803
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7432n223
Supporting Variantsnssv18279234
Samples
Known GenesNIPAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571959
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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