A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016691



Internal ID18759226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:107240508..107320070hg38UCSC Ensembl
Innerchr7:106880953..106960515hg19UCSC Ensembl
Innerchr7:106668189..106747751hg18UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3879563
hg1979563
hg1879563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6548n100
Supporting Variantsnssv3656212
Samples
Known GenesCOG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016691
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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