A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964547



Internal ID18253099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:36003423..36090261hg38UCSC Ensembl
Innerchr21:37375721..37462559hg19UCSC Ensembl
Innerchr21:36297591..36384429hg18UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3886839
hg1986839
hg1886839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2765867
SamplesHGDP01029
Known GenesCBR1, LOC100133286, SETD4
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964547
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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