A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697643



Internal ID18649238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105773532..105969062hg38UCSC Ensembl
Innerchr9:108535813..108731343hg19UCSC Ensembl
Innerchr9:107575634..107771164hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38195531
hg19195531
hg18195531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041073
Supporting Variants
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3697643
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer