A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360557



Internal ID22586226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15760449..15778094hg38UCSC Ensembl
chr10:15802448..15820093hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3817646
hg1917646
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978763
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360557
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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