A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551553



Internal ID16338962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:77926011..77927131hg38UCSC Ensembl
Innerchr10:79685769..79686889hg19UCSC Ensembl
Innerchr10:79355775..79356895hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381121
hg191121
hg181121
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1271n54
Supporting Variantsnssv751735
Samples
Known GenesDLG5, DLG5-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551553
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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