A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604236



Internal ID16044959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:95388284..95588040hg38UCSC Ensembl
Innerchr6:95836160..96035916hg19UCSC Ensembl
Innerchr6:95942881..96142637hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38199757
hg19199757
hg18199757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154852
SamplesNINDS_174
Known GenesMANEA, MANEA-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604236
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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