A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564262



Internal ID20937333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70757903..70766391hg38UCSC Ensembl
chr6:71467606..71476094hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg388489
hg198489
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274022
Samples
Known GenesSMAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564262
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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