A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591500



Internal ID16378909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:126296824..126357010hg38UCSC Ensembl
Innerchr3:126015667..126075853hg19UCSC Ensembl
Innerchr3:127498357..127558543hg18UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg3860187
hg1960187
hg1860187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv972406
Samples
Known GenesKLF15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591500
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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