A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536738



Internal ID20910081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167932541..167933233hg38UCSC Ensembl
chr1:167901779..167902471hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38693
hg19693
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248041
Samples
Known GenesMPC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536738
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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