A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv990876



Internal ID15938146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7195666..7221054hg38UCSC Ensembl
Innerchr4:7197393..7222781hg19UCSC Ensembl
Innerchr4:7248294..7273682hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3825389
hg1925389
hg1825389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593564
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)nssv990876
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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