A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv734108



Internal ID16028064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:197695775..197724907hg38UCSC Ensembl
Innerchr1:197664905..197694037hg19UCSC Ensembl
Innerchr1:195931528..195960660hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3829133
hg1929133
hg1829133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548873
Supporting Variants
Samples
Known GenesDENND1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv734108
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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