A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009743



Internal ID18752274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6640281..6683568hg38UCSC Ensembl
Innerchr3:6681968..6725255hg19UCSC Ensembl
Innerchr3:6656968..6700255hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3843288
hg1943288
hg1843288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591824
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009743
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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