A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542845



Internal ID20916096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67900125..67901798hg38UCSC Ensembl
chr1:68365808..68367481hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381674
hg191674
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251290
Samples
Known GenesGNG12-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542845
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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