A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001056



Internal ID18743587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:47870852..48182359hg38UCSC Ensembl
Innerchr3:47912342..48223849hg19UCSC Ensembl
Innerchr3:47887346..48198853hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38311508
hg19311508
hg18311508
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739873
Samples
Known GenesCDC25A, MAP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001056
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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