A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565301



Internal ID16352710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:82009652..82036025hg38UCSC Ensembl
Innerchr14:82475996..82502369hg19UCSC Ensembl
Innerchr14:81545749..81572122hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3826374
hg1926374
hg1826374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv830096
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565301
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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