A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174574



Internal ID15876125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:123668548..123688189hg38UCSC Ensembl
Innerchr10:125428064..125447705hg19UCSC Ensembl
Innerchr10:125418054..125437695hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3819642
hg1919642
hg1819642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552276
Supporting Variants
SamplesHGDP00787
Known GenesGPR26
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174574
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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