A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593559



Internal ID16034282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7151915..7195666hg38UCSC Ensembl
Innerchr4:7153642..7197393hg19UCSC Ensembl
Innerchr4:7204543..7248294hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3843752
hg1943752
hg1843752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8942n54
Supporting Variantsnssv990873
Samples
Known GenesSORCS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593559
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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