A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526953



Internal ID15454246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:70642494..71129481hg38UCSC Ensembl
Innerchr18:68309730..68796717hg19UCSC Ensembl
Innerchr18:66460710..66947697hg18UCSC Ensembl
Innerchr18:66460710..66947697hg17UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38486988
hg19486988
hg18486988
hg17486988
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703325
Samples
Known GenesGTSCR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526953
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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