A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519769



Internal ID15447062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:116262564..116265032hg38UCSC Ensembl
Innerchr10:118022076..118024544hg19UCSC Ensembl
Innerchr10:118012066..118014534hg18UCSC Ensembl
Innerchr10:118012066..118014534hg17UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg382469
hg192469
hg182469
hg172469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv675359, nssv658407
Samples
Known GenesGFRA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519769
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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