A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590728



Internal ID16378137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:76756867..76846692hg38UCSC Ensembl
Innerchr3:76806018..76895843hg19UCSC Ensembl
Innerchr3:76888708..76978533hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3889826
hg1989826
hg1889826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv965820
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590728
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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