A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057865



Internal ID19147084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12409110..12447619hg38UCSC Ensembl
Innerchr19:12519924..12558433hg19UCSC Ensembl
Innerchr19:12380924..12419433hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3838510
hg1938510
hg1838510
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3435n100
Supporting Variantsnssv3564759
Samples
Known GenesZNF443
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057865
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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