A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8899n54



Internal ID22776794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1601262..1602019hg38UCSC Ensembl
chr4:1602989..1603746hg19UCSC Ensembl
chr4:1572949..1573706hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38758
hg19758
hg18758
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593326, nsv593333, nsv593325, nsv593331
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8899n54
Frequency
Sample Size17421
Observed Gain36
Observed Loss506
Observed Complex0
Frequencyn/a


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