A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564794



Internal ID16352203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:47702127..47728456hg38UCSC Ensembl
Innerchr14:48171330..48197659hg19UCSC Ensembl
Innerchr14:47241080..47267409hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3826330
hg1926330
hg1826330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148616
SamplesHGDP01368
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564794
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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