A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149218



Internal ID15854413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24821213..24869979hg38UCSC Ensembl
Innerchr15:25066360..25115126hg19UCSC Ensembl
Innerchr15:22617453..22666219hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3848767
hg1948767
hg1848767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568532
Supporting Variants
Samples1780862101_A
Known GenesSNRPN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149218
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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