A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527436



Internal ID15454729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148422604..148446350hg38UCSC Ensembl
Innerchr7:148119696..148143442hg19UCSC Ensembl
Innerchr7:147750629..147774375hg18UCSC Ensembl
Innerchr7:147557344..147581090hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3823747
hg1923747
hg1823747
hg1723747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703876
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527436
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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