A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024713



Internal ID19113930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:159214650..159324697hg38UCSC Ensembl
Innerchr7:159007339..159117386hg19UCSC Ensembl
Innerchr7:158700100..158810147hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38110048
hg19110048
hg18110048
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6779n100
Supporting Variantsnssv3674808
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)nsv1024713
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