A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549865



Internal ID20923015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26240909..26241261hg38UCSC Ensembl
chr1:26567400..26567752hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251584
Samples
Known GenesCEP85
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549865
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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