A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601172



Internal ID16041895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:25451930..25451992hg38UCSC Ensembl
Innerchr6:25452158..25452220hg19UCSC Ensembl
Innerchr6:25560137..25560199hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3863
hg1963
hg1863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1051364, nssv1051366, nssv1051365, nssv1051363
Samples
Known GenesLRRC16A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601172
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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