A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550849



Internal ID20923990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173540629..173541705hg38UCSC Ensembl
chr2:174405357..174406433hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg381077
hg191077
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256125
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550849
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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