A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14249530



Internal ID21305952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25174845..25201209hg38UCSC Ensembl
Outerchr15:25172311..25205630hg38UCSC Ensembl
Innerchr15:25419992..25446356hg19UCSC Ensembl
Outerchr15:25417458..25450777hg19UCSC Ensembl
Innerchr15:22971085..22997449hg18UCSC Ensembl
Outerchr15:22968551..23001870hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3833320
hg1933320
hg1833320
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170245
Supporting Variants
SamplesNGO_24
Known GenesSNORD115-10, SNORD115-11, SNORD115-12, SNORD115-13, SNORD115-14, SNORD115-15, SNORD115-16, SNORD115-17, SNORD115-18, SNORD115-19, SNORD115-2, SNORD115-29, SNORD115-3, SNORD115-36, SNORD115-4, SNORD115-43, SNORD115-5, SNORD115-6, SNORD115-7, SNORD115-8, SNORD115-9
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14249530
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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