A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701008



Internal ID15090974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:24916118..24935412hg38UCSC Ensembl
Innerchr2:25138987..25158281hg19UCSC Ensembl
Innerchr2:24992491..25011785hg18UCSC Ensembl
Innerchr2:25050638..25069932hg17UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3819295
hg1919295
hg1819295
hg1719295
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524979
Supporting Variants
Samples
Known GenesADCY3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701008
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