A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520011



Internal ID15100618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:157678308..157703838hg38UCSC Ensembl
Innerchr1:157648098..157673628hg19UCSC Ensembl
Innerchr1:155914722..155940252hg18UCSC Ensembl
Innerchr1:154461171..154486701hg17UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3825531
hg1925531
hg1825531
hg1725531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697176
Samples
Known GenesFCRL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520011
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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