A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020986



Internal ID19110204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135622535..135650625hg38UCSC Ensembl
Innerchr7:135307283..135335373hg19UCSC Ensembl
Innerchr7:134957823..134985913hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3828091
hg1928091
hg1828091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3664231
Samples
Known GenesNUP205
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020986
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