A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564148



Internal ID16351557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27993073..28049942hg38UCSC Ensembl
Innerchr14:28462279..28519148hg19UCSC Ensembl
Innerchr14:27532119..27589002hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3856870
hg1956870
hg1856884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3598n54
Supporting Variantsnssv825085, nssv825088, nssv1149488, nssv825087, nssv825086
SamplesHGDP00630
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564148
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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