A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14252496



Internal ID21310117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32212063..32220019hg38UCSC Ensembl
Outerchr15:32197052..32239115hg38UCSC Ensembl
Innerchr15:32504264..32512220hg19UCSC Ensembl
Outerchr15:32489253..32531316hg19UCSC Ensembl
Innerchr15:30291556..30299512hg18UCSC Ensembl
Outerchr15:30276545..30318608hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3842064
hg1942064
hg1842064
Variant TypeCNV deletion
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170275
Supporting Variants
SamplesNGO_55
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14252496
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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