A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565184



Internal ID16352593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74338468..74403135hg38UCSC Ensembl
Innerchr14:74805171..74869838hg19UCSC Ensembl
Innerchr14:73874924..73939591hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3864668
hg1964668
hg1864668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv829519
Samples
Known GenesVRTN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565184
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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