A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574132



Internal ID20947203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149669088..149669889hg38UCSC Ensembl
chr6:149990224..149991025hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6449n223
Supporting Variantsnssv18269284
Samples
Known GenesLATS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574132
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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