A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv991226



Internal ID15938496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7941379..7967867hg38UCSC Ensembl
Innerchr4:7943106..7969594hg19UCSC Ensembl
Innerchr4:7994006..8020494hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3826489
hg1926489
hg1826489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593621
Supporting Variants
Samples
Known GenesABLIM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv991226
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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