A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589571



Internal ID16376980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:7030551..7128324hg38UCSC Ensembl
Innerchr3:7072238..7170011hg19UCSC Ensembl
Innerchr3:7047238..7145011hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3897774
hg1997774
hg1897774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8204n54
Supporting Variantsnssv958605
Samples
Known GenesGRM7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589571
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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