A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562041



Internal ID20935112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42738856..42739291hg38UCSC Ensembl
chr6:42706594..42707029hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271318
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562041
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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