A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719872



Internal ID15667142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103610478..103644798hg38UCSC Ensembl
Innerchr1:104153100..104187420hg19UCSC Ensembl
Innerchr1:103954623..103988943hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3834321
hg1934321
hg1834321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547034
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)nssv719872
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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