A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056764



Internal ID19145983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10504328..10775598hg38UCSC Ensembl
Innerchr21:10736859..11008129hg19UCSC Ensembl
Innerchr21:9758730..10030000hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38271271
hg19271271
hg18271271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4353n100
Supporting Variantsnssv3583684
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)nsv1056764
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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