A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522953



Internal ID15450246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130901156..130904061hg38UCSC Ensembl
Innerchr9:133776543..133779448hg19UCSC Ensembl
Innerchr9:132766364..132769269hg18UCSC Ensembl
Innerchr9:130806097..130809002hg17UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg382906
hg192906
hg182906
hg172906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698621
Samples
Known GenesFIBCD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522953
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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