A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545453



Internal ID18843734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25170021..25207565hg38UCSC Ensembl
Innerchr15:25415168..25452712hg19UCSC Ensembl
Innerchr15:22966261..23003805hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3837545
hg1937545
hg1837545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045043
Supporting Variants
Samples
Known GenesSNORD115-1, 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, SNORD115-29, SNORD115-3, SNORD115-36, SNORD115-4, SNORD115-43, SNORD115-5, SNORD115-6, SNORD115-7, SNORD115-8, SNORD115-9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3545453
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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