A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681848



Internal ID15418500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46287904hg38UCSC Ensembl
Innerchr10:47543322..47659140hg19UCSC Ensembl
Innerchr10:47013328..47129146hg18UCSC Ensembl
Innerchr10:47013328..47129146hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38115819
hg19115819
hg18115819
hg17115819
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516485
Supporting Variants
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681848
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