A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542585



Internal ID20915843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207772591..207777564hg38UCSC Ensembl
chr1:207945936..207950909hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg384974
hg194974
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250032
Samples
Known GenesCD46
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542585
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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