A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688794



Internal ID18987075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30199762..30497205hg38UCSC Ensembl
Innerchr9:30199760..30497203hg19UCSC Ensembl
Innerchr9:30189760..30487203hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38297444
hg19297444
hg18297444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016740
Supporting Variants
Samples
Known GenesLOC401497
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3688794
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