A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv827829



Internal ID16121785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:47728456..47811079hg38UCSC Ensembl
Innerchr14:48197659..48280282hg19UCSC Ensembl
Innerchr14:47267409..47350032hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3882624
hg1982624
hg1882624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564795
Supporting Variants
Samples
Known GenesLINC00648, MIR548Y
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv827829
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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