A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094190



Internal ID21507765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19240629..21558840hg38UCSC Ensembl
chr17:19143942..21462103hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg382318212
hg192318162
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670902
Supporting Variants
SamplesNA20509
Known GenesAKAP10, ALDH3A1, ALDH3A2, B9D1, C17orf103, C17orf51, CCDC144CP, CCDC144NL, CDRT15L2, DHRS7B, EPN2, EPN2-AS1, EPN2-IT1, KCNJ12, KCNJ18, KRT16P3, LGALS9B, LOC100287072, LOC440416, MAP2K3, MAPK7, MFAP4, MIR1180, RNF112, SLC47A1, SLC47A2, SNORA59A, SNORA59B, SPECC1, TMEM11, ULK2, USP22
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094190
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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