A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593624



Internal ID16034347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:8024449..8046246hg38UCSC Ensembl
Innerchr4:8026176..8047973hg19UCSC Ensembl
Innerchr4:8077076..8098873hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3821798
hg1921798
hg1821798
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv991229
Samples
Known GenesABLIM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593624
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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