A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568217



Internal ID18866498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40257932..40275453hg38UCSC Ensembl
Innerchr19:40763839..40781360hg19UCSC Ensembl
Innerchr19:45455679..45473200hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3817522
hg1917522
hg1817522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059884
Supporting Variants
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)nssv3568217
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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