A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589702



Internal ID18887983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41052589..41103534hg38UCSC Ensembl
Innerchr3:41094080..41145025hg19UCSC Ensembl
Innerchr3:41069084..41120029hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3850946
hg1950946
hg1850946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000021
Supporting Variants
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)nssv3589702
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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