A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032278



Internal ID18774812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40057772..40356701hg38UCSC Ensembl
Innerchr7:40097371..40396300hg19UCSC Ensembl
Innerchr7:40063896..40362825hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38298930
hg19298930
hg18298930
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643871
Samples
Known GenesC7orf10, CDK13, MPLKIP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032278
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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