A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557530



Internal ID20930601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94933602..94934502hg38UCSC Ensembl
chr8:95945830..95946730hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279142
Samples
Known GenesTP53INP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557530
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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