A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356039



Internal ID22581708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119814116..119815291hg38UCSC Ensembl
chr10:121573628..121574803hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381176
hg191176
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969862
Supporting Variants
Samples
Known GenesINPP5F
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356039
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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