A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050526



Internal ID19139745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:35126475..35145640hg38UCSC Ensembl
Innerchr15:35418676..35437841hg19UCSC Ensembl
Innerchr15:33205968..33225133hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3819166
hg1919166
hg1819166
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552229
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)nsv1050526
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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