A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018668



Internal ID19107885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62506780..62925225hg38UCSC Ensembl
Innerchr7:61875418..62385603hg19UCSC Ensembl
Innerchr7:61512853..62023038hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38418446
hg19510186
hg18510186
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6403n100
Supporting Variantsnssv3661761
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)nsv1018668
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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