A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759823



Internal ID19058104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:120196924..120275786hg38UCSC Ensembl
Innerchr9:122959202..123038064hg19UCSC Ensembl
Innerchr9:121999023..122077885hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3878863
hg1978863
hg1878863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048345
Supporting Variants
Samples
Known GenesMIR147A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3759823
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