A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169433



Internal ID21313916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43592920..43703690hg38UCSC Ensembl
Outerchr15:43553305..43719842hg38UCSC Ensembl
Innerchr15:43885118..43995888hg19UCSC Ensembl
Outerchr15:43845503..44012040hg19UCSC Ensembl
Innerchr15:41672410..41783180hg18UCSC Ensembl
Outerchr15:41632795..41799332hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38166538
hg19166538
hg18166538
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248889, nssv14250087, nssv14246189, nssv14240872, nssv14251401
SamplesSNI_7, MLY_16, NGO_48, SNI_14
Known GenesCATSPER2, CKMT1A, CKMT1B, PPIP5K1, RNU6-28P, STRC
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169433
Frequency
Sample Size93
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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