A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051620



Internal ID19140839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:52433765..52534114hg38UCSC Ensembl
Innerchr14:52900483..53000832hg19UCSC Ensembl
Innerchr14:51970233..52070582hg18UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38100350
hg19100350
hg18100350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531022
Samples
Known GenesTXNDC16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051620
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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