A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036202



Internal ID18778733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110967076..111021655hg38UCSC Ensembl
Innerchr10:112726834..112781413hg19UCSC Ensembl
Innerchr10:112716824..112771403hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3854580
hg1954580
hg1854580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv975n100
Supporting Variantsnssv3503433
Samples
Known GenesSHOC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036202
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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