A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018998



Internal ID19108215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:54117556..54129851hg38UCSC Ensembl
Innerchr7:54185249..54197544hg19UCSC Ensembl
Innerchr7:54152743..54165038hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3812296
hg1912296
hg1812296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6354n100
Supporting Variantsnssv3661311
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018998
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