A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605616



Internal ID16393025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:191859..193914hg38UCSC Ensembl
Innerchr7:191859..193914hg19UCSC Ensembl
Innerchr7:286942..288997hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg382056
hg192056
hg182056
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11094n54
Supporting Variantsnssv1077674, nssv1077675
Samples
Known GenesFAM20C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605616
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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