A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014889



Internal ID18757424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103635404..103764624hg38UCSC Ensembl
Innerchr1:104178026..104307246hg19UCSC Ensembl
Innerchr1:103979549..104108769hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38129221
hg19129221
hg18129221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv226n100
Supporting Variantsnssv3498196
Samples
Known GenesAMY1A, AMY1B, AMY1C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014889
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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