A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577975



Internal ID16365384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:95981..209307hg38UCSC Ensembl
Innerchr19:95981..209307hg19UCSC Ensembl
Innerchr19:46981..160307hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38113327
hg19113327
hg18113327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv890327, nssv890328
Samples
Known GenesLINC01002, OR4F17
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577975
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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