A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044486



Internal ID18787017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68312766..68349135hg38UCSC Ensembl
Innerchr15:68605104..68641473hg19UCSC Ensembl
Innerchr15:66392158..66428527hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3836370
hg1936370
hg1836370
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2616n100
Supporting Variantsnssv3553658
Samples
Known GenesITGA11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044486
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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