A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591227



Internal ID16378636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:104936738..104996194hg38UCSC Ensembl
Innerchr3:104655582..104715038hg19UCSC Ensembl
Innerchr3:106138272..106197728hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3859457
hg1959457
hg1859457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152514
SamplesNINDS_172
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591227
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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