A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554328



Internal ID20927430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:111836091..111836477hg38UCSC Ensembl
chr2:112593668..112594054hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256492
Samples
Known GenesANAPC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554328
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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