A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030559



Internal ID19119778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:54118769..54129851hg38UCSC Ensembl
Innerchr7:54186462..54197544hg19UCSC Ensembl
Innerchr7:54153956..54165038hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3811083
hg1911083
hg1811083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6354n100
Supporting Variantsnssv3661318, nssv3661316, nssv3661317
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)nsv1030559
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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