A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv990881



Internal ID15938151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7309672..7331425hg38UCSC Ensembl
Innerchr4:7311399..7333152hg19UCSC Ensembl
Innerchr4:7362300..7384053hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3821754
hg1921754
hg1821754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593570
Supporting Variants
Samples
Known GenesMIR4798, SORCS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv990881
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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