A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549538



Internal ID20922699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96571119..96571872hg38UCSC Ensembl
chr1:97036675..97037428hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv275n223
Supporting Variantsnssv18253986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549538
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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