A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061350



Internal ID18803881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44364917..44531444hg38UCSC Ensembl
Innerchr19:44869075..45035469hg19UCSC Ensembl
Innerchr19:49560915..49727309hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38166528
hg19166395
hg18166395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3573781
Samples
Known GenesCEACAM20, ZNF180, ZNF229, ZNF285
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061350
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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