A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606051



Internal ID16046774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:8140216..8413683hg38UCSC Ensembl
Innerchr7:8179846..8453313hg19UCSC Ensembl
Innerchr7:8146371..8419838hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38273468
hg19273468
hg18273468
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11178n54
Supporting Variantsnssv1078886
Samples
Known GenesICA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606051
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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