A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683652



Internal ID15073618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:41349351..41366519hg38UCSC Ensembl
Innerchr22:41745355..41762523hg19UCSC Ensembl
Innerchr22:40075301..40092469hg18UCSC Ensembl
Innerchr22:40069855..40087023hg17UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3817169
hg1917169
hg1817169
hg1717169
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516925
Supporting Variants
Samples
Known GenesZC3H7B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683652
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