A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689027



Internal ID15078993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:18925345..18931063hg38UCSC Ensembl
Innerchr9:18925343..18931061hg19UCSC Ensembl
Innerchr9:18915343..18921061hg18UCSC Ensembl
Innerchr9:18915343..18921061hg17UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg385719
hg195719
hg185719
hg175719
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519384
Supporting Variants
Samples
Known GenesFAM154A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689027
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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