A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14246977



Internal ID21312290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32217691..32240890hg38UCSC Ensembl
Outerchr15:32212063..32247336hg38UCSC Ensembl
Innerchr15:32509892..32533091hg19UCSC Ensembl
Outerchr15:32504264..32539537hg19UCSC Ensembl
Innerchr15:30297184..30320383hg18UCSC Ensembl
Outerchr15:30291556..30326829hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3835274
hg1935274
hg1835274
Variant TypeCNV deletion
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170275
Supporting Variants
SamplesSNI_16
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14246977
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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