A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611851



Internal ID16052574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:107212459..107473684hg38UCSC Ensembl
Innerchr8:108224687..108485912hg19UCSC Ensembl
Innerchr8:108293863..108555088hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38261226
hg19261226
hg18261226
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1118243
Samples
Known GenesANGPT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611851
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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