A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697648



Internal ID18995929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107785976..107934972hg38UCSC Ensembl
Innerchr9:110548257..110697253hg19UCSC Ensembl
Innerchr9:109588078..109737074hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38148997
hg19148997
hg18148997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051101
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3697648
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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