A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543657



Internal ID20916903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20513717..20514601hg38UCSC Ensembl
chr1:20840210..20841094hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38885
hg19885
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249964
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543657
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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