A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591565



Internal ID16378974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:127117314..127141881hg38UCSC Ensembl
Innerchr3:126836157..126860724hg19UCSC Ensembl
Innerchr3:128318847..128343414hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3824568
hg1924568
hg1824568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv972922
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591565
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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