A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555169



Internal ID20928259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179474960..179478327hg38UCSC Ensembl
chr1:179444095..179447462hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg383368
hg193368
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv453n223
Supporting Variantsnssv18248829
Samples
Known GenesAXDND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555169
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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