A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059430



Internal ID19148649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10558280..10643715hg38UCSC Ensembl
Innerchr21:10868742..10954177hg19UCSC Ensembl
Innerchr21:9890613..9976048hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3885436
hg1985436
hg1885436
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3585015
Samples
Known GenesTPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059430
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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