A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026081



Internal ID18768613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:50458202..50470486hg38UCSC Ensembl
Innerchr7:50525900..50538184hg19UCSC Ensembl
Innerchr7:50493394..50505678hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3812285
hg1912285
hg1812285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661265
Samples
Known GenesDDC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026081
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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