A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719764



Internal ID16013720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103579055..103591836hg38UCSC Ensembl
Innerchr1:104121677..104134458hg19UCSC Ensembl
Innerchr1:103923200..103935981hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3812782
hg1912782
hg1812782
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546980
Supporting Variants
Samples
Known GenesAMY2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv719764
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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