A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554230



Internal ID20927336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37481459..37484570hg38UCSC Ensembl
chr1:37947060..37950171hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383112
hg193112
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251068
Samples
Known GenesZC3H12A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554230
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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