A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013540



Internal ID19102758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:33210111..33244582hg38UCSC Ensembl
Innerchr3:33251603..33286074hg19UCSC Ensembl
Innerchr3:33226607..33261078hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3834472
hg1934472
hg1834472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589588
Samples
Known GenesSUSD5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013540
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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