A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606227



Internal ID16393636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12389862..12486656hg38UCSC Ensembl
Innerchr7:12429488..12526282hg19UCSC Ensembl
Innerchr7:12396013..12492807hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3896795
hg1996795
hg1896795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11207n54
Supporting Variantsnssv1079184
Samples
Known GenesVWDE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606227
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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