A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354700



Internal ID22580369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33996548..34013322hg38UCSC Ensembl
chr10:34285476..34302250hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3816775
hg1916775
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978190
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354700
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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