A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665702



Internal ID21614007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101895317..101981188hg38UCSC Ensembl
chr15:102435520..102521391hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3885872
hg1985872
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095189
SamplesHG00731
Known GenesDDX11L9, FAM138E, MIR6859-1, MIR6859-2, OR4F4, WASH3P
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665702
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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