A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549990



Internal ID20923141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182123795..182124184hg38UCSC Ensembl
chr1:182092930..182093319hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249463
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549990
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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