A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704558



Internal ID15441210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46287904..46330334hg38UCSC Ensembl
Innerchr10:47659140..47701570hg19UCSC Ensembl
Innerchr10:47129146..47171576hg18UCSC Ensembl
Innerchr10:47129146..47171576hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3842431
hg1942431
hg1842431
hg1742431
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516485
Supporting Variants
Samples
Known GenesANTXRL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704558
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