A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564674



Internal ID18862955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8680583..8717236hg38UCSC Ensembl
Innerchr19:8790846..8827581hg19UCSC Ensembl
Innerchr19:8651846..8688581hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3836654
hg1936736
hg1836736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060576
Supporting Variants
Samples
Known GenesACTL9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564674
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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