A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519212



Internal ID15099819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9070235..9089765hg38UCSC Ensembl
Innerchr17:8973552..8993082hg19UCSC Ensembl
Innerchr17:8914277..8933807hg18UCSC Ensembl
Innerchr17:8914277..8933807hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3819531
hg1919531
hg1819531
hg1719531
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696701
Samples
Known GenesNTN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519212
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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