A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543567



Internal ID20916813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24747994..24748581hg38UCSC Ensembl
chr1:25074485..25075072hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv128n223
Supporting Variantsnssv18251510
Samples
Known GenesCLIC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543567
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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