A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv968101



Internal ID16262057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:96360020..96494261hg38UCSC Ensembl
Innerchr3:96078864..96213105hg19UCSC Ensembl
Innerchr3:97561554..97695795hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38134242
hg19134242
hg18134242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591037
Supporting Variants
Samples
Known GenesMIR8060
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv968101
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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