A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014652



Internal ID19103870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:127384997..127472066hg38UCSC Ensembl
Innerchr3:127103840..127190909hg19UCSC Ensembl
Innerchr3:128586530..128673599hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3887070
hg1987070
hg1887070
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3603498
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)nsv1014652
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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