A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042954



Internal ID19132173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24847119..24870013hg38UCSC Ensembl
Innerchr15:25092266..25115160hg19UCSC Ensembl
Innerchr15:22643359..22666253hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3822895
hg1922895
hg1822895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2473n100
Supporting Variantsnssv3721465
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)nsv1042954
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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