A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704667



Internal ID15441319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132216219..132251071hg38UCSC Ensembl
Innerchr9:135091606..135126458hg19UCSC Ensembl
Innerchr9:134081427..134116279hg18UCSC Ensembl
Innerchr9:132121160..132156012hg17UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3834853
hg1934853
hg1834853
hg1734853
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528123
Supporting Variants
Samples
Known GenesNTNG2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704667
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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