A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592757



Internal ID16380166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:188205927..188407553hg38UCSC Ensembl
Innerchr3:187923715..188125341hg19UCSC Ensembl
Innerchr3:189406409..189608035hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38201627
hg19201627
hg18201627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152570
Samples1780862101_A
Known GenesLPP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592757
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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