A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553472



Internal ID20926581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61025925..61026495hg38UCSC Ensembl
chr1:61491597..61492167hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250455
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553472
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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