A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv738111



Internal ID16032067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:234039208..234120311hg38UCSC Ensembl
Innerchr1:234174954..234256057hg19UCSC Ensembl
Innerchr1:232241577..232322680hg18UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3881104
hg1981104
hg1881104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549364
Supporting Variants
Samples
Known GenesSLC35F3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv738111
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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