A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601184



Internal ID16041907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26379309..26451325hg38UCSC Ensembl
Innerchr6:26379537..26451553hg19UCSC Ensembl
Innerchr6:26487516..26559532hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3872017
hg1972017
hg1872017
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1051391
Samples
Known GenesBTN2A2, BTN2A3P, BTN3A1, BTN3A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601184
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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