A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048209



Internal ID18790740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96616946..96636733hg38UCSC Ensembl
Innerchr14:97083283..97103070hg19UCSC Ensembl
Innerchr14:96153036..96172823hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3819788
hg1919788
hg1819788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532633
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)nsv1048209
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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