A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057052



Internal ID18799583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40270221..40283859hg38UCSC Ensembl
Innerchr19:40776128..40789766hg19UCSC Ensembl
Innerchr19:45467968..45481606hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3813639
hg1913639
hg1813639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568218
Samples
Known GenesAKT2, MIR641
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057052
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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