A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556037



Internal ID20929108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118996871..118997238hg38UCSC Ensembl
chr6:119318036..119318403hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268611
Samples
Known GenesFAM184A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556037
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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