A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026963



Internal ID19116181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109339142..109463293hg38UCSC Ensembl
Innerchr7:108979199..109103350hg19UCSC Ensembl
Innerchr7:108766435..108890586hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38124152
hg19124152
hg18124152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3656230, nssv3656229
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026963
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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