A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604854



Internal ID16392263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:151002528..151015304hg38UCSC Ensembl
Innerchr6:151323664..151336440hg19UCSC Ensembl
Innerchr6:151365357..151378133hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3812777
hg1912777
hg1812777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155798
SamplesHGDP01380
Known GenesMTHFD1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604854
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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