A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052499



Internal ID18795030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96508187..96568468hg38UCSC Ensembl
Innerchr14:96974524..97034805hg19UCSC Ensembl
Innerchr14:96044277..96104558hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3860282
hg1960282
hg1860282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532627
Samples
Known GenesPAPOLA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052499
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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