A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053932



Internal ID19143151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22162256..22477390hg38UCSC Ensembl
Innerchr14:22630152..22946380hg19UCSC Ensembl
Innerchr14:21699992..22016220hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38315135
hg19316229
hg18316229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1805n100
Supporting Variantsnssv3532224
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)nsv1053932
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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