A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539676



Internal ID20912971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:113127650..113128973hg38UCSC Ensembl
chr1:113670272..113671595hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg381324
hg191324
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247466
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539676
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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