A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008287



Internal ID19097506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:29139628..29165971hg38UCSC Ensembl
Innerchr3:29181119..29207462hg19UCSC Ensembl
Innerchr3:29156123..29182466hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3826344
hg1926344
hg1826344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589580
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)nsv1008287
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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