A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759786



Internal ID19058067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93599766..93635056hg38UCSC Ensembl
Innerchr9:96362048..96397338hg19UCSC Ensembl
Innerchr9:95401869..95437159hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3835291
hg1935291
hg1835291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044461
Supporting Variants
Samples
Known GenesPHF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3759786
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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