A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522893



Internal ID15450186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:91494107..91581358hg38UCSC Ensembl
Innerchr7:91123422..91210673hg19UCSC Ensembl
Innerchr7:90961358..91048609hg18UCSC Ensembl
Innerchr7:90768073..90855324hg17UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3887252
hg1987252
hg1887252
hg1787252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698551
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522893
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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