A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002707



Internal ID18745239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3858107..4139829hg38UCSC Ensembl
Innerchr3:3899791..4181513hg19UCSC Ensembl
Innerchr3:3874791..4156513hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38281723
hg19281723
hg18281723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590390, nssv3590391
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)nsv1002707
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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