A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548243



Internal ID20921439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9216153..9216744hg38UCSC Ensembl
chr1:9276212..9276803hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252672
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548243
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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