A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610588



Internal ID16397997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16092262..16163959hg38UCSC Ensembl
Innerchr8:15949771..16021468hg19UCSC Ensembl
Innerchr8:15994142..16065839hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3871698
hg1971698
hg1871698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12022n54
Supporting Variantsnssv1106972, nssv1106975, nssv1106969, nssv1156335, nssv1106973, nssv1106974, nssv1106977, nssv1106970, nssv1106979, nssv1106976, nssv1156336, nssv1106978, nssv1106971
SamplesHGDP00524, 1780862041_A
Known GenesMSR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610588
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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