A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552213



Internal ID20925341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38865648..38866198hg38UCSC Ensembl
chr1:39331320..39331870hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252417
Samples
Known GenesGJA9-MYCBP, MYCBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552213
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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