A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057670



Internal ID19146889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10556317..10753328hg38UCSC Ensembl
Innerchr21:10759129..10956140hg19UCSC Ensembl
Innerchr21:9781000..9978011hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38197012
hg19197012
hg18197012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4350n100
Supporting Variantsnssv3585008, nssv3732528, nssv3732527, nssv3732526, nssv3585007
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)nsv1057670
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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