A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062755



Internal ID18805286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40231556..40252328hg38UCSC Ensembl
Innerchr19:40737463..40758235hg19UCSC Ensembl
Innerchr19:45429303..45450075hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3820773
hg1920773
hg1820773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568211, nssv3568212
Samples
Known GenesAKT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062755
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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