A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv720004



Internal ID15667274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103612150..103618188hg38UCSC Ensembl
Innerchr1:104154772..104160810hg19UCSC Ensembl
Innerchr1:103956295..103962333hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg386039
hg196039
hg186039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547070
Supporting Variants
Samples
Known GenesAMY2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv720004
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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