A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129329



Internal ID18920698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:84191211..84403668hg38UCSC Ensembl
Outerchr15:84859963..84958366hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38212458
hg1998404
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962762
SamplesKWS1
Known GenesGOLGA6L4, LOC388152, LOC440300, LOC642423
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129329
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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