A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546441



Internal ID20919660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:210653466..210653542hg38UCSC Ensembl
chr1:210826810..210826886hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247865
Samples
Known GenesHHAT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546441
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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