A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517178



Internal ID15444471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76535987..76549730hg38UCSC Ensembl
Innerchr9:79150903..79164646hg19UCSC Ensembl
Innerchr9:78340723..78354466hg18UCSC Ensembl
Innerchr9:76380457..76394200hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3813744
hg1913744
hg1813744
hg1713744
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv653935, nssv677399, nssv654838, nssv683444, nssv692021, nssv677565, nssv670575, nssv668371, nssv666707, nssv652737, nssv655462, nssv679068, nssv669843, nssv659909
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517178
Frequency
Sample Size2026
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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