A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv744096



Internal ID16038052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14970536..15018884hg38UCSC Ensembl
Innerchr10:15012535..15060883hg19UCSC Ensembl
Innerchr10:15052541..15100889hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3848349
hg1948349
hg1848349
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550012
Supporting Variants
Samples
Known GenesMEIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv744096
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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