A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174271



Internal ID15880019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121010407..121025489hg38UCSC Ensembl
Innerchr10:122769920..122785002hg19UCSC Ensembl
Innerchr10:122759910..122774992hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3815083
hg1915083
hg1815083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552230
Supporting Variants
SamplesNINDS_142
Known GenesMIR5694
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174271
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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