A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528913



Internal ID15109520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:12657720..12677103hg38UCSC Ensembl
Innerchr12:12810654..12830037hg19UCSC Ensembl
Innerchr12:12701921..12721304hg18UCSC Ensembl
Innerchr12:12701921..12721304hg17UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg3819384
hg1919384
hg1819384
hg1719384
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv89n21
Supporting Variantsnssv705598
Samples
Known GenesGPR19
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528913
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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