A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560376



Internal ID20933447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42492165..42492707hg38UCSC Ensembl
chr8:42349683..42350225hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278044
Samples
Known GenesSLC20A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560376
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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