A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697097



Internal ID15087063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132164169..132175336hg38UCSC Ensembl
Innerchr9:135039556..135050723hg19UCSC Ensembl
Innerchr9:134029377..134040544hg18UCSC Ensembl
Innerchr9:132069110..132080277hg17UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3811168
hg1911168
hg1811168
hg1711168
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519872
Supporting Variants
Samples
Known GenesNTNG2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697097
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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