A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570949



Internal ID20944020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29570559..29571858hg38UCSC Ensembl
chr8:29428076..29429375hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7306n223
Supporting Variantsnssv18277659
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570949
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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