A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522627



Internal ID15449920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:14536321..14564182hg38UCSC Ensembl
Innerchr21:15908642..15936503hg19UCSC Ensembl
Innerchr21:14830513..14858374hg18UCSC Ensembl
Innerchr21:14830513..14858374hg17UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3827862
hg1927862
hg1827862
hg1727862
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706025
Samples
Known GenesSAMSN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522627
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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