A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4548n54



Internal ID22772443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55963576..56045329hg38UCSC Ensembl
chr15:56255774..56337527hg19UCSC Ensembl
chr15:54043066..54124819hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3881754
hg1981754
hg1881754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569544, nsv569545, nsv569546, nsv569543
Samples1780862416_A, 1780862101_A
Known GenesNEDD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4548n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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