A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537040



Internal ID20910379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201997953..201999084hg38UCSC Ensembl
chr1:201967081..201968212hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381132
hg191132
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248895
Samples
Known GenesRNPEP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537040
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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