A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021962



Internal ID22083593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158765365..158854282hg38UCSC Ensembl
Outerchr7:158763744..158858465hg38UCSC Ensembl
Innerchr7:158558056..158646973hg19UCSC Ensembl
Outerchr7:158556435..158651156hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3894722
hg1994722
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156770
Supporting Variants
Samples
Known GenesESYT2, WDR60
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021962
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