A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056792



Internal ID19146011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:23026821..23386261hg38UCSC Ensembl
Innerchr21:24399143..24758582hg19UCSC Ensembl
Innerchr21:23321014..23680453hg18UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg38359441
hg19359440
hg18359440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599977
Samples
Known GenesD21S2088E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056792
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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