A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539438



Internal ID20912733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8240935..8242206hg38UCSC Ensembl
chr1:8300995..8302266hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg381272
hg191272
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253892
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539438
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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