A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706236



Internal ID19004517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:109445261..109574018hg38UCSC Ensembl
Innerchr10:111205019..111333776hg19UCSC Ensembl
Innerchr10:111195009..111323766hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38128758
hg19128758
hg18128758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046386
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3706236
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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