A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577078



Internal ID20950149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43214812..43220310hg38UCSC Ensembl
chr17:41366831..41372330hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg385499
hg195500
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242280
Samples
Known GenesTMEM106A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577078
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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