A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057950



Internal ID19147169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10504189..10775598hg38UCSC Ensembl
Innerchr21:10736859..11008268hg19UCSC Ensembl
Innerchr21:9758730..10030139hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38271410
hg19271410
hg18271410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4353n100
Supporting Variantsnssv3583686, nssv3583685
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)nsv1057950
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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