A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021790



Internal ID22083421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154601461..154609123hg38UCSC Ensembl
Outerchr7:154598185..154609307hg38UCSC Ensembl
Innerchr7:154393171..154400833hg19UCSC Ensembl
Outerchr7:154389895..154401017hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3811123
hg1911123
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156764
Supporting Variants
Samples
Known GenesDPP6
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021790
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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