A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034941



Internal ID19124161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88503095..88617790hg38UCSC Ensembl
Innerchr7:88132410..88247104hg19UCSC Ensembl
Innerchr7:87970346..88085040hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38114696
hg19114695
hg18114695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6524n100
Supporting Variantsnssv3655192
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)nsv1034941
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