A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549211



Internal ID20922379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32261813..32262560hg38UCSC Ensembl
chr1:32727414..32728161hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38748
hg19748
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv150n223
Supporting Variantsnssv18250827
Samples
Known GenesLCK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549211
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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