A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565525



Internal ID16352934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:92704648..92752613hg38UCSC Ensembl
Innerchr14:93170993..93218958hg19UCSC Ensembl
Innerchr14:92240746..92288711hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3847966
hg1947966
hg1847966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149540
Samples1780862300_A
Known GenesLGMN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565525
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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