A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014021



Internal ID19103241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:158836826..158917333hg38UCSC Ensembl
Innerchr3:158554615..158635122hg19UCSC Ensembl
Innerchr3:160037309..160117816hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3880508
hg1980508
hg1880508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606399
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)nsv1014021
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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