A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062092



Internal ID19151311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:27821868..27987620hg38UCSC Ensembl
Innerchr21:29194187..29359939hg19UCSC Ensembl
Innerchr21:28116058..28281810hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38165753
hg19165753
hg18165753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4422n100
Supporting Variantsnssv3732694, nssv3600103
Samples
Known GenesMIR5009
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062092
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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