A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522248



Internal ID15102855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:159577325..159580247hg38UCSC Ensembl
Innerchr3:159295114..159298036hg19UCSC Ensembl
Innerchr3:160777808..160780730hg18UCSC Ensembl
Innerchr3:160777816..160780738hg17UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg382923
hg192923
hg182923
hg172923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695028
Samples
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522248
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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