A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034411



Internal ID19123633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13703740..13787131hg38UCSC Ensembl
Innerchr7:13743365..13826756hg19UCSC Ensembl
Innerchr7:13709890..13793281hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3883392
hg1983392
hg1883392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643148
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)nsv1034411
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