A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv988441



Internal ID15935711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1797575..1806167hg38UCSC Ensembl
Innerchr4:1799302..1807894hg19UCSC Ensembl
Innerchr4:1769100..1777692hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg388593
hg198593
hg188593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593337
Supporting Variants
Samples
Known GenesFGFR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv988441
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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