A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016709



Internal ID19105926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155174804..155197793hg38UCSC Ensembl
Innerchr7:154966514..154989503hg19UCSC Ensembl
Innerchr7:154597447..154620436hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3822990
hg1922990
hg1822990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6764n100
Supporting Variantsnssv3674678, nssv3674676, nssv3674677
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)nsv1016709
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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