A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042176



Internal ID19131395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:91751700..91786034hg38UCSC Ensembl
Innerchr15:92294930..92329264hg19UCSC Ensembl
Innerchr15:90095934..90130268hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3834335
hg1934335
hg1834335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555223
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)nsv1042176
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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