A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549893



Internal ID16337302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5659798..5679690hg38UCSC Ensembl
Innerchr10:5701761..5721653hg19UCSC Ensembl
Innerchr10:5741767..5761659hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3819893
hg1919893
hg1819893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743477
Samples
Known GenesASB13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549893
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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