A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018890



Internal ID19108107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38517832..38561344hg38UCSC Ensembl
Innerchr7:38557432..38600944hg19UCSC Ensembl
Innerchr7:38523957..38567469hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3843513
hg1943513
hg1843513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643865
Samples
Known GenesAMPH
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018890
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