A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578805



Internal ID16366214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20100731..20449142hg38UCSC Ensembl
Innerchr19:20211540..20631948hg19UCSC Ensembl
Innerchr19:20072540..20423788hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38348412
hg19420409
hg18351249
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv896162
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF486, ZNF826P, ZNF90
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578805
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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