A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028914



Internal ID19118133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:133722836..133978125hg38UCSC Ensembl
Innerchr7:133407589..133662878hg19UCSC Ensembl
Innerchr7:133058129..133313418hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38255290
hg19255290
hg18255290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3662214
Samples
Known GenesEXOC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028914
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