A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006471



Internal ID18749002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21344135..21555463hg38UCSC Ensembl
Innerchr3:21385627..21596955hg19UCSC Ensembl
Innerchr3:21360631..21571959hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38211329
hg19211329
hg18211329
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593147
Samples
Known GenesVENTXP7, ZNF385D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006471
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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