A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057118



Internal ID18799649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52692173..52977196hg38UCSC Ensembl
Innerchr19:53195426..53480449hg19UCSC Ensembl
Innerchr19:57887238..58172261hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38285024
hg19285024
hg18285024
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3572065
Samples
Known GenesZNF28, ZNF320, ZNF321P, ZNF468, ZNF600, ZNF611, ZNF702P, ZNF816, ZNF816-ZNF321P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057118
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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