A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156660



Internal ID22087061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40914664..40948290hg38UCSC Ensembl
Outerchr7:40912809..40964726hg38UCSC Ensembl
Innerchr7:40954263..40987889hg19UCSC Ensembl
Outerchr7:40952408..41004325hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3851918
hg1951918
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021106
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156660
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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