A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521698



Internal ID15102305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94570993..94575939hg38UCSC Ensembl
Innerchr9:97333275..97338221hg19UCSC Ensembl
Innerchr9:96373096..96378042hg18UCSC Ensembl
Innerchr9:94412830..94417776hg17UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg384947
hg194947
hg184947
hg174947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698320
Samples
Known GenesFBP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521698
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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