A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698890



Internal ID15088856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103500563..103586151hg38UCSC Ensembl
Innerchr1:104043185..104128773hg19UCSC Ensembl
Innerchr1:103815773..103930296hg18UCSC Ensembl
Innerchr1:103755206..103840794hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3885589
hg1985589
hg18114524
hg1785589
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523177
Supporting Variants
Samples
Known GenesACTG1P4, AMY2B, LOC101928436, RNPC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698890
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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