A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604998



Internal ID16392407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160610992..160634892hg38UCSC Ensembl
Innerchr6:161032024..161055924hg19UCSC Ensembl
Innerchr6:160952014..160975914hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3823901
hg1923901
hg1823901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075170
Samples
Known GenesLPA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604998
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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