A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610679



Internal ID16051402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17401289..17417200hg38UCSC Ensembl
Innerchr8:17258798..17274709hg19UCSC Ensembl
Innerchr8:17303169..17319080hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3815912
hg1915912
hg1815912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1107310
Samples
Known GenesMTMR7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610679
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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