A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663230



Internal ID15399882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46314592hg38UCSC Ensembl
Innerchr10:47543322..47685828hg19UCSC Ensembl
Innerchr10:47013328..47155834hg18UCSC Ensembl
Innerchr10:47013328..47155834hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38142507
hg19142507
hg18142507
hg17142507
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)nssv663230
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