A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696146



Internal ID18994427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64493516..64965592hg38UCSC Ensembl
Innerchr9:69505934..69978010hg19UCSC Ensembl
Innerchr9:68795754..69267830hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38472077
hg19472077
hg18472077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033836
Supporting Variants
Samples
Known GenesLOC100133920
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696146
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