A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571421



Internal ID20944492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38746950..38747403hg38UCSC Ensembl
chr6:38714726..38715179hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38454
hg19454
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271398
Samples
Known GenesDNAH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571421
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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