A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042525



Internal ID18785056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103411867..103541050hg38UCSC Ensembl
Innerchr10:105171624..105300807hg19UCSC Ensembl
Innerchr10:105161614..105290797hg18UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38129184
hg19129184
hg18129184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv966n100
Supporting Variantsnssv3511192
Samples
Known GenesCALHM1, CALHM2, CALHM3, NEURL1, PDCD11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042525
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer