A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7701n100



Internal ID20159317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112604798..112828670hg38UCSC Ensembl
chr9:115367078..115590950hg19UCSC Ensembl
chr9:114406899..114630771hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38223873
hg19223873
hg18223873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035169, nsv1038999, nsv1044381, nsv1051808, nsv1041424, nsv1048327, nsv1044168, nsv1049451, nsv1047374
Samples
Known GenesINIP, KIAA1958, SNX30
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7701n100
Frequency
Sample Size29084
Observed Gain48
Observed Loss0
Observed Complex0
Frequencyn/a


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