A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv982663



Internal ID16276619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:188009727..188016711hg38UCSC Ensembl
Innerchr3:187727515..187734499hg19UCSC Ensembl
Innerchr3:189210209..189217193hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg386985
hg196985
hg186985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592717
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv982663
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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