A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037114



Internal ID19126333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:81656971..81775332hg38UCSC Ensembl
Innerchr14:82123315..82241676hg19UCSC Ensembl
Innerchr14:81193068..81311429hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38118362
hg19118362
hg18118362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531228
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037114
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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