A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604803



Internal ID16392212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:143548539..143551173hg38UCSC Ensembl
Innerchr6:143869676..143872310hg19UCSC Ensembl
Innerchr6:143911369..143914003hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg382635
hg192635
hg182635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10956n54
Supporting Variantsnssv1074150
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604803
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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