A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539734



Internal ID20913029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244030422..244031276hg38UCSC Ensembl
chr1:244193724..244194578hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250203
Samples
Known GenesLOC339529
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539734
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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