A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537839



Internal ID20911171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:99947677..99948337hg38UCSC Ensembl
chr1:100413233..100413893hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv279n223
Supporting Variantsnssv18252832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537839
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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