A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063780



Internal ID19152999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44392222..44426631hg38UCSC Ensembl
Innerchr19:44896386..44930803hg19UCSC Ensembl
Innerchr19:49588226..49622643hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3834410
hg1934418
hg1834418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3605n100
Supporting Variantsnssv3573784
Samples
Known GenesZNF229, ZNF285
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063780
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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