A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519199



Internal ID15099806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:159531034..159541335hg38UCSC Ensembl
Innerchr3:159248823..159259124hg19UCSC Ensembl
Innerchr3:160731517..160741818hg18UCSC Ensembl
Innerchr3:160731525..160741826hg17UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg3810302
hg1910302
hg1810302
hg1710302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696684
Samples
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519199
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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