A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528041



Internal ID15108648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:180185641..180194255hg38UCSC Ensembl
Innerchr1:180154776..180163390hg19UCSC Ensembl
Innerchr1:178421399..178430013hg18UCSC Ensembl
Innerchr1:176886433..176895047hg17UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg388615
hg198615
hg188615
hg178615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704573
Samples
Known GenesQSOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528041
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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