A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546080



Internal ID20875250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169154095..169154495hg38UCSC Ensembl
chr1:169123333..169123733hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248069
Samples
Known GenesNME7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546080
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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