A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522032



Internal ID15449325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:103799524..103805114hg38UCSC Ensembl
Innerchr2:104415982..104421572hg19UCSC Ensembl
Innerchr2:103782414..103788004hg18UCSC Ensembl
Innerchr2:103874500..103880090hg17UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg385591
hg195591
hg185591
hg175591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694801
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522032
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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