A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053655



Internal ID19142874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23802041..23822436hg38UCSC Ensembl
Innerchr15:24047188..24067583hg19UCSC Ensembl
Innerchr15:21598281..21618676hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3820396
hg1920396
hg1820396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2411n100
Supporting Variantsnssv3538888
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)nsv1053655
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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