A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567864



Internal ID20940935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109778846..111235585hg38UCSC Ensembl
chr6:110100049..111556788hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381456740
hg191456740
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267823
Samples
Known GenesAMD1, CDC40, CDK19, DDO, FIG4, GPR6, GSTM2P1, GTF3C6, METTL24, RPF2, SLC16A10, SLC22A16, WASF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567864
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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