A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020516



Internal ID19109735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:136282664..136298936hg38UCSC Ensembl
Innerchr7:135967412..135983684hg19UCSC Ensembl
Innerchr7:135617952..135634224hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3816273
hg1916273
hg1816273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6639n100
Supporting Variantsnssv3664236
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)nsv1020516
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