A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052199



Internal ID18794730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26334093..26735737hg38UCSC Ensembl
Innerchr14:26803299..27204943hg19UCSC Ensembl
Innerchr14:25873139..26274783hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38401645
hg19401645
hg18401645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528539
Samples
Known GenesNOVA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052199
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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