A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027702



Internal ID19116921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:67257116..67376926hg38UCSC Ensembl
Innerchr7:66722103..66841913hg19UCSC Ensembl
Innerchr7:66359538..66479348hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38119811
hg19119811
hg18119811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6447n100
Supporting Variantsnssv3655630
Samples
Known GenesLOC101929736, PMS2P4, STAG3L4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027702
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