A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610678



Internal ID16051401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17361120..17488285hg38UCSC Ensembl
Innerchr8:17218629..17345794hg19UCSC Ensembl
Innerchr8:17263000..17390156hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38127166
hg19127166
hg18127157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156347
Samples1780854487_A
Known GenesMTMR7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610678
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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