A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550787



Internal ID15991510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46233054..46259024hg38UCSC Ensembl
Innerchr10:47604290..47630260hg19UCSC Ensembl
Innerchr10:47074296..47100266hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3825971
hg1925971
hg1825971
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv747629
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550787
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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