A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525649



Internal ID15106256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:124553087..124588577hg38UCSC Ensembl
Innerchr8:125565328..125600818hg19UCSC Ensembl
Innerchr8:125634509..125669999hg18UCSC Ensembl
Innerchr8:125634509..125669999hg17UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3835491
hg1935491
hg1835491
hg1735491
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701803
Samples
Known GenesMTSS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525649
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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