A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569544



Internal ID16356953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55981248..56028037hg38UCSC Ensembl
Innerchr15:56273446..56320235hg19UCSC Ensembl
Innerchr15:54060738..54107527hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3846790
hg1946790
hg1846790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4548n54
Supporting Variantsnssv1148879
Samples1780862101_A
Known GenesNEDD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569544
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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