A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604978



Internal ID16392387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:157671606..157694755hg38UCSC Ensembl
Innerchr6:158092638..158115787hg19UCSC Ensembl
Innerchr6:158012626..158035775hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3823150
hg1923150
hg1823150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10984n54
Supporting Variantsnssv1155100
SamplesHGDP00830
Known GenesZDHHC14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604978
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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