A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600871



Internal ID16041594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4904146..5171775hg38UCSC Ensembl
Innerchr6:4904380..5172009hg19UCSC Ensembl
Innerchr6:4849379..5117008hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38267630
hg19267630
hg18267630
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154024
SamplesNINDS_125
Known GenesCDYL, LYRM4, MIR3691, PPP1R3G, RPP40
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600871
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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