A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046800



Internal ID19136019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87602537..87621031hg38UCSC Ensembl
Innerchr15:88145768..88164262hg19UCSC Ensembl
Innerchr15:85946772..85965266hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3818495
hg1918495
hg1818495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555193
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)nsv1046800
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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