A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678208



Internal ID15068174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127271203..127271936hg38UCSC Ensembl
Innerchr9:130033482..130034215hg19UCSC Ensembl
Innerchr9:129073303..129074036hg18UCSC Ensembl
Innerchr9:127113036..127113769hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38734
hg19734
hg18734
hg17734
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516966
Supporting Variants
Samples
Known GenesGARNL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678208
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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