A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547803



Internal ID20921003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150584495..150585085hg38UCSC Ensembl
chr1:150556971..150557561hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247530
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547803
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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