A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591352



Internal ID16378761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119010267..119083007hg38UCSC Ensembl
Innerchr3:118729114..118801854hg19UCSC Ensembl
Innerchr3:120211804..120284544hg18UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg3872741
hg1972741
hg1872741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8517n54
Supporting Variantsnssv971648, nssv971646, nssv971647, nssv971643, nssv971642, nssv971645, nssv971649, nssv1152533, nssv971644
SamplesNINDS_99
Known GenesIGSF11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591352
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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