A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3721464



Internal ID19019745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24824408..24853826hg38UCSC Ensembl
Innerchr15:25069555..25098973hg19UCSC Ensembl
Innerchr15:22620648..22650066hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3829419
hg1929419
hg1829419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051660
Supporting Variants
Samples
Known GenesSNRPN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3721464
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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