A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568744



Internal ID16356153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30355183..30440634hg38UCSC Ensembl
Innerchr15:30647386..30732837hg19UCSC Ensembl
Innerchr15:28434678..28520129hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3885452
hg1985452
hg1885452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4423n54
Supporting Variantsnssv839473
Samples
Known GenesCHRFAM7A, LOC101059918
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568744
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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