A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538432



Internal ID20911749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173469848..173470877hg38UCSC Ensembl
chr1:173438987..173440016hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg381030
hg191030
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248109
Samples
Known GenesLOC100506023
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538432
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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