A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14243706



Internal ID21306593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30595753..30796274hg38UCSC Ensembl
Outerchr15:30529555..30807423hg38UCSC Ensembl
Innerchr15:30887956..31088477hg19UCSC Ensembl
Outerchr15:30821758..31099626hg19UCSC Ensembl
Innerchr15:28675248..28875769hg18UCSC Ensembl
Outerchr15:28609050..28886918hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38277869
hg19277869
hg18277869
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169498
Supporting Variants
SamplesNGO_29
Known GenesARHGAP11B, GOLGA8H, LOC100288637, ULK4P1, ULK4P2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14243706
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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