A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604775



Internal ID16392184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:140627290..140897923hg38UCSC Ensembl
Innerchr6:140948427..141219060hg19UCSC Ensembl
Innerchr6:140990120..141260753hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38270634
hg19270634
hg18270634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1073810
Samples
Known GenesMIR4465
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604775
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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