A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549764



Internal ID16337173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:625555..658520hg38UCSC Ensembl
Innerchr10:671495..704460hg19UCSC Ensembl
Innerchr10:661495..694460hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3832966
hg1932966
hg1832966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv740164
Samples
Known GenesDIP2C, MIR5699, PRR26
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549764
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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