A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005860



Internal ID18748391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103621153..103714945hg38UCSC Ensembl
Innerchr1:104163775..104257567hg19UCSC Ensembl
Innerchr1:103965298..104059090hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3893793
hg1993793
hg1893793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv224n100
Supporting Variantsnssv3501812
Samples
Known GenesAMY1A, AMY1B, AMY1C, AMY2A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005860
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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