A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552200



Internal ID20925328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:231272714..231273261hg38UCSC Ensembl
chr1:231408460..231409007hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38548
hg19548
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250354
Samples
Known GenesGNPAT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552200
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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