A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527829



Internal ID15108436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9882590..9925703hg38UCSC Ensembl
Innerchr18:9882587..9925700hg19UCSC Ensembl
Innerchr18:9872587..9915700hg18UCSC Ensembl
Innerchr18:9872587..9915700hg17UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3843114
hg1943114
hg1843114
hg1743114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704325
Samples
Known GenesTXNDC2, VAPA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527829
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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