A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702147



Internal ID15438799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:26845501..26850107hg38UCSC Ensembl
Innerchr22:27241464..27246070hg19UCSC Ensembl
Innerchr22:25571464..25576070hg18UCSC Ensembl
Innerchr22:25566018..25570624hg17UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg384607
hg194607
hg184607
hg174607
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525941
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702147
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