A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663691



Internal ID15053657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:154095720..154151047hg38UCSC Ensembl
Innerchr1:154068196..154123523hg19UCSC Ensembl
Innerchr1:152334820..152390147hg18UCSC Ensembl
Innerchr1:150881269..150936596hg17UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3855328
hg1955328
hg1855328
hg1755328
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520398
Supporting Variants
Samples
Known GenesNUP210L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663691
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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