A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118560



Internal ID18923265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:75255559..75301059hg38UCSC Ensembl
Outerchr15:75547900..75593400hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3845501
hg1945501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1242n106
Supporting Variantsnssv3959070
SamplesKWS1
Known GenesGOLGA6C, GOLGA6D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118560
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer