A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17432949



Internal ID22490819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:47732141..47733551hg38UCSC Ensembl
chr6:47699877..47701287hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg381411
hg191411
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972377
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17432949
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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