A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538008



Internal ID20911334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100435773..100436590hg38UCSC Ensembl
chr1:100901329..100902146hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38818
hg19818
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv280n223
Supporting Variantsnssv18249194
Samples
Known GenesCDC14A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538008
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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