A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697602



Internal ID18649197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103000721..103050888hg38UCSC Ensembl
Innerchr9:105763003..105813170hg19UCSC Ensembl
Innerchr9:104802824..104852991hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3850168
hg1950168
hg1850168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039024
Supporting Variants
Samples
Known GenesCYLC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3697602
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