A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv749369



Internal ID16043325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65141812..65251930hg38UCSC Ensembl
Innerchr10:66901570..67011688hg19UCSC Ensembl
Innerchr10:66571576..66681694hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38110119
hg19110119
hg18110119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551241
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)nssv749369
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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