A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570136



Internal ID20943207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:14876268..15184522hg38UCSC Ensembl
chr8:14733777..15042031hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38308255
hg19308255
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277337
Samples
Known GenesSGCZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570136
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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