A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056203



Internal ID18798734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57481818..57504613hg38UCSC Ensembl
Innerchr19:57993186..58015981hg19UCSC Ensembl
Innerchr19:62684998..62707793hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3822796
hg1922796
hg1822796
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3570453
Samples
Known GenesZNF419, ZNF773
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056203
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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