A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv827705



Internal ID16121661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:47228599..47248595hg38UCSC Ensembl
Innerchr14:47697802..47717798hg19UCSC Ensembl
Innerchr14:46767552..46787548hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3819997
hg1919997
hg1819997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564773
Supporting Variants
Samples
Known GenesMDGA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv827705
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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