A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603632



Internal ID16391041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:69036162..69071894hg38UCSC Ensembl
Innerchr6:69746054..69781786hg19UCSC Ensembl
Innerchr6:69802775..69838507hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3835733
hg1935733
hg1835733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10757n54
Supporting Variantsnssv1154807
SamplesHGDP00635
Known GenesBAI3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603632
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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