A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437114



Internal ID22494984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36238245..37822315hg38UCSC Ensembl
chr9:36238242..37822312hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg381584071
hg191584071
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972210
Supporting Variants
Samples
Known GenesDCAF10, EXOSC3, FBXO10, FRMPD1, GNE, GRHPR, LOC100506710, MELK, MIR4475, MIR4476, MIR4540, PAX5, POLR1E, RNF38, TOMM5, TRMT10B, ZBTB5, ZCCHC7
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437114
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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