A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004701



Internal ID18747232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103560154..103635404hg38UCSC Ensembl
Innerchr1:104102776..104178026hg19UCSC Ensembl
Innerchr1:103904299..103979549hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3875251
hg1975251
hg1875251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv216n100
Supporting Variantsnssv3470887, nssv3466627, nssv3474049, nssv3464339
Samples
Known GenesACTG1P4, AMY2A, AMY2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004701
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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