A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049916



Internal ID19139135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76161853..76198206hg38UCSC Ensembl
Innerchr15:76454194..76490547hg19UCSC Ensembl
Innerchr15:74241249..74277602hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3836354
hg1936354
hg1836354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2625n100
Supporting Variantsnssv3553740
Samples
Known GenesC15orf27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049916
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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