A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv746936



Internal ID16040892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38576045..38643693hg38UCSC Ensembl
Innerchr10:38869176..38936824hg19UCSC Ensembl
Innerchr10:38909182..38976830hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3867649
hg1967649
hg1867649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550472
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv746936
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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