A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604980



Internal ID16392389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:158032896..158046957hg38UCSC Ensembl
Innerchr6:158453928..158467989hg19UCSC Ensembl
Innerchr6:158373916..158387977hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3814062
hg1914062
hg1814062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1074985
Samples
Known GenesSYNJ2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604980
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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