A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550701



Internal ID20923841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:144222360..144222711hg38UCSC Ensembl
chr2:144979927..144980278hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254495
Samples
Known GenesGTDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550701
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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