A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv761615



Internal ID16055571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:131112246..131113741hg38UCSC Ensembl
Innerchr10:132910509..132912004hg19UCSC Ensembl
Innerchr10:132800499..132801994hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381496
hg191496
hg181496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552437
Supporting Variants
Samples
Known GenesTCERG1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv761615
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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