A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3517118



Internal ID18468713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110964401..111035401hg38UCSC Ensembl
Innerchr10:112724159..112795159hg19UCSC Ensembl
Innerchr10:112714149..112785149hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3871001
hg1971001
hg1871001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048444
Supporting Variants
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)nssv3517118
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