A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011686



Internal ID19100903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:130072354..130125697hg38UCSC Ensembl
Innerchr3:129791197..129844540hg19UCSC Ensembl
Innerchr3:131273887..131327230hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3853344
hg1953344
hg1853344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4898n100
Supporting Variantsnssv3607052
Samples
Known GenesALG1L2, FAM86HP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011686
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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