A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057627



Internal ID19146846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38742206..38780053hg38UCSC Ensembl
Innerchr21:40114130..40151977hg19UCSC Ensembl
Innerchr21:39036000..39073847hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3837848
hg1937848
hg1837848
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4432n100
Supporting Variantsnssv3733449
Samples
Known GenesLINC00114
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057627
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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