A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv990877



Internal ID15938147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7218206..7263908hg38UCSC Ensembl
Innerchr4:7219933..7265635hg19UCSC Ensembl
Innerchr4:7270834..7316536hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3845703
hg1945703
hg1845703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593565
Supporting Variants
Samples
Known GenesSORCS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv990877
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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