A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053638



Internal ID19142857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:57483520..57522019hg38UCSC Ensembl
Innerchr14:57950238..57988737hg19UCSC Ensembl
Innerchr14:57019991..57058490hg18UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3838500
hg1938500
hg1838500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531039
Samples
Known GenesC14orf105
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053638
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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