A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525153



Internal ID15452446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:195897320..195961866hg38UCSC Ensembl
Innerchr1:195866450..195930996hg19UCSC Ensembl
Innerchr1:194133073..194197619hg18UCSC Ensembl
Innerchr1:192598107..192662653hg17UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3864547
hg1964547
hg1864547
hg1764547
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701225
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525153
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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