A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036749



Internal ID18779280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77591684..77620066hg38UCSC Ensembl
Innerchr15:77884026..77912408hg19UCSC Ensembl
Innerchr15:75671081..75699463hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3828383
hg1928383
hg1828383
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3554588
Samples
Known GenesLINGO1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036749
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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