A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv760375



Internal ID16054331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122457306..122457745hg38UCSC Ensembl
Innerchr10:124216822..124217261hg19UCSC Ensembl
Innerchr10:124206812..124207251hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38440
hg19440
hg18440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552252
Supporting Variants
Samples
Known GenesARMS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv760375
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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