A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554102



Internal ID20927211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:144222102..144222836hg38UCSC Ensembl
chr2:144979669..144980403hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254494
Samples
Known GenesGTDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554102
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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