A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047081



Internal ID19136300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:91607931..91648109hg38UCSC Ensembl
Innerchr15:92151161..92191339hg19UCSC Ensembl
Innerchr15:89952165..89992343hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3840179
hg1940179
hg1840179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555221
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)nsv1047081
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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