A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565622



Internal ID16353031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94342423..94375205hg38UCSC Ensembl
Innerchr14:94808760..94841542hg19UCSC Ensembl
Innerchr14:93878513..93911295hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3832783
hg1932783
hg1832783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148961
SamplesNINDS_60
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565622
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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