A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047047



Internal ID19136266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49778027..49832899hg38UCSC Ensembl
Innerchr15:50070224..50125096hg19UCSC Ensembl
Innerchr15:47857516..47912388hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3854873
hg1954873
hg1854873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2593n100
Supporting Variantsnssv3552385
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)nsv1047047
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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