A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524937



Internal ID15105544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73790158..73933937hg38UCSC Ensembl
Innerchr10:75549916..75693695hg19UCSC Ensembl
Innerchr10:75219922..75363701hg18UCSC Ensembl
Innerchr10:75219922..75363701hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38143780
hg19143780
hg18143780
hg17143780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv46n21
Supporting Variantsnssv700951
Samples
Known GenesC10orf55, CAMK2G, NDST2, PLAU, ZSWIM8, ZSWIM8-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524937
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