A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14248565



Internal ID21303946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:39296025..39299987hg38UCSC Ensembl
Outerchr15:39295103..39305425hg38UCSC Ensembl
Innerchr15:39588226..39592188hg19UCSC Ensembl
Outerchr15:39587304..39597626hg19UCSC Ensembl
Innerchr15:37375518..37379480hg18UCSC Ensembl
Outerchr15:37374596..37384918hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3810323
hg1910323
hg1810323
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169591
Supporting Variants
SamplesNGO_1
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14248565
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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