A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053565



Internal ID19142784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:87247696..87318103hg38UCSC Ensembl
Innerchr14:87714040..87784447hg19UCSC Ensembl
Innerchr14:86783793..86854200hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3870408
hg1970408
hg1870408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532555
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)nsv1053565
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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