A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522878



Internal ID15450171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102486606..102535489hg38UCSC Ensembl
Innerchr14:102952943..103001826hg19UCSC Ensembl
Innerchr14:102022696..102071579hg18UCSC Ensembl
Innerchr14:102022696..102071579hg17UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3848884
hg1948884
hg1848884
hg1748884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698533
Samples
Known GenesANKRD9, TECPR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522878
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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