A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719620



Internal ID16013576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:95789509..95819075hg38UCSC Ensembl
Innerchr1:96255065..96284631hg19UCSC Ensembl
Innerchr1:96027653..96057219hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3829567
hg1929567
hg1829567
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546859
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv719620
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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