A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604851



Internal ID16392260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150601979..150620174hg38UCSC Ensembl
Innerchr6:150923115..150941310hg19UCSC Ensembl
Innerchr6:150964808..150983003hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3818196
hg1918196
hg1818196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155797
SamplesHGDP00534
Known GenesPLEKHG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604851
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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