A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752214



Internal ID16046170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86341610..86368524hg38UCSC Ensembl
Innerchr10:88101367..88128281hg19UCSC Ensembl
Innerchr10:88091347..88118261hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3826915
hg1926915
hg1826915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551774
Supporting Variants
Samples
Known GenesGRID1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv752214
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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