A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125363



Internal ID19276431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:85681719..85697288hg38UCSC Ensembl
Outerchr15:86224950..86240519hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3815570
hg1915570
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983538
SamplesKWS2
Known GenesAKAP13
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125363
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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