A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538200



Internal ID20911523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52394966..52395434hg38UCSC Ensembl
chr1:52860638..52861106hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249718
Samples
Known GenesORC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538200
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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