A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589725



Internal ID16377134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13054032..13098468hg38UCSC Ensembl
Innerchr3:13095532..13139968hg19UCSC Ensembl
Innerchr3:13070532..13114968hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3844437
hg1944437
hg1844437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151881
Samples1780862043_A
Known GenesIQSEC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589725
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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