A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044972



Internal ID19134191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87353113..87366979hg38UCSC Ensembl
Innerchr15:87896344..87910210hg19UCSC Ensembl
Innerchr15:85697348..85711214hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3813867
hg1913867
hg1813867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2656n100
Supporting Variantsnssv3555186, nssv3555187
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044972
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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