A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009028



Internal ID18751559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103576471..103725588hg38UCSC Ensembl
Innerchr1:104119093..104268210hg19UCSC Ensembl
Innerchr1:103920616..104069733hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38149118
hg19149118
hg18149118
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv218n100
Supporting Variantsnssv3464512, nssv3473918, nssv3466785
Samples
Known GenesAMY1A, AMY1B, AMY1C, 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)nsv1009028
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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