A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000699



Internal ID19089916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14210406..14242039hg38UCSC Ensembl
Innerchr3:14251906..14283539hg19UCSC Ensembl
Innerchr3:14226910..14258543hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3831634
hg1931634
hg1831634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593087
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)nsv1000699
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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