A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14249814



Internal ID21305847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25170021..25252170hg38UCSC Ensembl
Outerchr15:25165735..25254781hg38UCSC Ensembl
Innerchr15:25415168..25497317hg19UCSC Ensembl
Outerchr15:25410882..25499928hg19UCSC Ensembl
Innerchr15:22966261..23048410hg18UCSC Ensembl
Outerchr15:22961975..23051021hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3889047
hg1989047
hg1889047
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170245
Supporting Variants
SamplesNGO_23
Known GenesPWAR4, SNORD115-1, SNORD115-10, SNORD115-11, SNORD115-12, SNORD115-13, SNORD115-14, SNORD115-15, SNORD115-16, SNORD115-17, SNORD115-18, SNORD115-19, SNORD115-2, SNORD115-20, SNORD115-21, SNORD115-22, SNORD115-23, SNORD115-24, SNORD115-25, SNORD115-26, SNORD115-27, SNORD115-28, SNORD115-29, SNORD115-3, SNORD115-30, SNORD115-31, SNORD115-32, SNORD115-33, SNORD115-34, SNORD115-35, SNORD115-36, SNORD115-37, SNORD115-38, SNORD115-39, SNORD115-4, SNORD115-40, SNORD115-41, SNORD115-42, SNORD115-43, SNORD115-44, 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)nssv14249814
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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