A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011717



Internal ID19100935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153921849..153970905hg38UCSC Ensembl
Innerchr3:153639638..153688694hg19UCSC Ensembl
Innerchr3:155122328..155171384hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3849057
hg1949057
hg1849057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4924n100
Supporting Variantsnssv3606344
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)nsv1011717
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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