A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3522711



Internal ID18820992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43003719..43036583hg38UCSC Ensembl
Innerchr10:43499167..43532031hg19UCSC Ensembl
Innerchr10:42819173..42852037hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3832865
hg1932865
hg1832865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054604
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)nssv3522711
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