A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539665



Internal ID20912961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150274665..150275209hg38UCSC Ensembl
chr1:150247070..150247617hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg38545
hg19548
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247516
Samples
Known GenesC1orf54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539665
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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