A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538262



Internal ID20911583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41057618..41057989hg38UCSC Ensembl
chr1:41523290..41523661hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250958
Samples
Known GenesSCMH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538262
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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