A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603446



Internal ID16390855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65604257..65630539hg38UCSC Ensembl
Innerchr6:66314150..66340432hg19UCSC Ensembl
Innerchr6:66370871..66397153hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3826283
hg1926283
hg1826283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10729n54
Supporting Variantsnssv1153712
SamplesNINDS_46
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603446
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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