A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006256



Internal ID18748787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103556018..103615675hg38UCSC Ensembl
Innerchr1:104098640..104158297hg19UCSC Ensembl
Innerchr1:103900163..103959820hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3859658
hg1959658
hg1859658
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv215n100
Supporting Variantsnssv3476004, nssv3699618
Samples
Known GenesACTG1P4, AMY2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006256
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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