A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696165



Internal ID18994446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64683555..64945771hg38UCSC Ensembl
Innerchr9:69695973..69958189hg19UCSC Ensembl
Innerchr9:68985793..69248009hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38262217
hg19262217
hg18262217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018703
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)nssv3696165
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